{"description":"Documents matching 'must include detailed description type'","count":10000,"total_pages":50,"next_page_url":"https://www.federalregister.gov/api/v1/documents?conditions%5Bterm%5D=must+include+detailed+description+type&format=json&page=2","results":[{"title":"Airworthiness Directives; DAHER AEROSPACE (Type Certificate Previously Held by SOCATA) Airplanes","type":"Rule","abstract":"The FAA is superseding Airworthiness Directive (AD) 2007-06-11 (AD 2007-06-11) for certain SOCATA (type certificate now held by DAHER AEROSPACE) Model TBM 700 airplanes. AD 2007-06-11 required repetitively inspecting the vertical stabilizer attachment fittings and bolts for cracks or corrosion, and, if necessary, repairing or replacing the damaged part and then applying a corrosion protection reinforcement. Since the FAA issued AD 2007-06-11, the European Union Aviation Safety Agency (EASA), which is the Technical Agent for the Member States of the European Union, superseded the previous Direction generale de l'aviation civile (DGAC) France AD to introduce new service information providing instructions for installing new vertical stabilizer attachment fittings having improved corrosion resistant material as an optional terminating action for the repetitive inspections. This AD retains the requirements of AD 2007-06-11 and includes a new optional terminating action for the repetitive inspections. The FAA is issuing this AD to address the unsafe condition on these products.","document_number":"2026-00162","html_url":"https://www.federalregister.gov/documents/2026/01/08/2026-00162/airworthiness-directives-daher-aerospace-type-certificate-previously-held-by-socata-airplanes","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-01-08/pdf/2026-00162.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-00162.pdf?1767793514","publication_date":"2026-01-08","agencies":[{"raw_name":"DEPARTMENT OF TRANSPORTATION","name":"Transportation Department","id":492,"url":"https://www.federalregister.gov/agencies/transportation-department","json_url":"https://www.federalregister.gov/api/v1/agencies/492","parent_id":null,"slug":"transportation-department"},{"raw_name":"Federal Aviation Administration","name":"Federal Aviation Administration","id":159,"url":"https://www.federalregister.gov/agencies/federal-aviation-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/159","parent_id":492,"slug":"federal-aviation-administration"}],"excerpts":"the following new airworthiness directive: \n \n \n 2025-26-02 DAHER AEROSPACE (<span class=\"match\">Type</span> Certificate previously held by SOCATA): \n Amendment 39-23224; Docket No. FAA-2025-2265; Project Identifier MCAI-2024-00714-A.\n \n (a) Effective Date \n This airworthiness directive (AD) is effective February 12, 2026. \n (b) Affected ADs \n This AD replaces AD 2007-06-11, Amendment 39-14992 (72 FR 12546, March 16, 2007) (AD 2007-06-11). \n (c) Applicability \n This AD applies to DAHER AEROSPACE (<span class=\"match\">type</span> certificate previously held by SOCATA) Model TBM 700 airplanes, manufacturer"},{"title":"Airworthiness Directives; DAHER AEROSPACE (Type Certificate Previously Held by SOCATA) Airplanes","type":"Proposed Rule","abstract":"The FAA proposes to supersede Airworthiness Directive (AD) 2007-06-11, which applies to certain SOCATA (type certificate now held by DAHER AEROSPACE) Model TBM 700 airplanes. AD 2007-06-11 requires repetitively inspecting the vertical stabilizer attachment fittings and bolts for cracks or corrosion, and, if necessary, repairing or replacing the damaged part and then applying a corrosion protection reinforcement. Since the FAA issued AD 2007-06-11, the European Union Aviation Safety Agency (EASA), which is the Technical Agent for the Member States of the European Union, superseded the previous Direction generale de l'aviation civile (DGAC) France AD to introduce new service information providing instructions for installing new vertical stabilizer attachment fittings having improved corrosion resistant material as an optional terminating action for the repetitive inspections. This proposed AD would retain the requirements of AD 2007- 06-11 and include a new optional terminating action for the repetitive inspections. The FAA is proposing this AD to address the unsafe condition on these products.","document_number":"2025-16263","html_url":"https://www.federalregister.gov/documents/2025/08/25/2025-16263/airworthiness-directives-daher-aerospace-type-certificate-previously-held-by-socata-airplanes","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-08-25/pdf/2025-16263.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-16263.pdf?1755866734","publication_date":"2025-08-25","agencies":[{"raw_name":"DEPARTMENT OF TRANSPORTATION","name":"Transportation Department","id":492,"url":"https://www.federalregister.gov/agencies/transportation-department","json_url":"https://www.federalregister.gov/api/v1/agencies/492","parent_id":null,"slug":"transportation-department"},{"raw_name":"Federal Aviation Administration","name":"Federal Aviation Administration","id":159,"url":"https://www.federalregister.gov/agencies/federal-aviation-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/159","parent_id":492,"slug":"federal-aviation-administration"}],"excerpts":"Adding the following new airworthiness directive: \n \n \n DAHER AEROSPACE (<span class=\"match\">Type</span> Certificate previously held by SOCATA): \n Docket No. FAA-2025-2265; Project Identifier MCAI-2024-00714-A.\n \n (a) Comments Due Date \n The FAA <span class=\"match\">must</span> receive comments on this airworthiness directive (AD) by October 9, 2025. \n (b) Affected ADs \n This AD replaces AD 2007-06-11, Amendment 39-14992 (72 FR 12546, dated March 16, 2007) (AD 2007-06-11). \n (c) Applicability \n This AD applies to DAHER AEROSPACE (<span class=\"match\">type</span> certificate previously held by SOCATA) Model TBM 700 airplanes, manufacturer"},{"title":"Application of the Federal Securities Laws to Certain Types of Crypto Assets and Certain Transactions Involving Crypto Assets","type":"Rule","abstract":"The Securities and Exchange Commission (\"Commission\" or \"SEC\") issues herein an interpretation regarding the application of the Federal securities laws to certain types of crypto assets and certain transactions involving crypto assets. The references in this release to \"we\" and \"our\" are to the Commission. The Commodity Futures Trading Commission (\"CFTC\") provides herein guidance relating to that interpretation.","document_number":"2026-05635","html_url":"https://www.federalregister.gov/documents/2026/03/23/2026-05635/application-of-the-federal-securities-laws-to-certain-types-of-crypto-assets-and-certain","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-03-23/pdf/2026-05635.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-05635.pdf?1774010720","publication_date":"2026-03-23","agencies":[{"raw_name":"COMMODITY FUTURES TRADING COMMISSION","name":"Commodity Futures Trading Commission","id":77,"url":"https://www.federalregister.gov/agencies/commodity-futures-trading-commission","json_url":"https://www.federalregister.gov/api/v1/agencies/77","parent_id":null,"slug":"commodity-futures-trading-commission"},{"raw_name":"SECURITIES AND EXCHANGE COMMISSION","name":"Securities and Exchange Commission","id":466,"url":"https://www.federalregister.gov/agencies/securities-and-exchange-commission","json_url":"https://www.federalregister.gov/api/v1/agencies/466","parent_id":null,"slug":"securities-and-exchange-commission"}],"excerpts":"as an investment.” \n 26 \n \n While the definition of “security” <span class=\"match\">includes</span> an enumerated list of “the commonly known documents traded for speculation or investment,” including “stock,” “bond,” and “note,” it also <span class=\"match\">includes</span> instruments “of a more variable character,” such as “investment contract,” “certificate of interest or participation in a profit-sharing agreement,” and “any interest or instrument commonly known as a security.” \n 27 \n \n In addition, the definition of “security” <span class=\"match\">includes</span> any “receipt for, guarantee of, or warrant or right to subscribe"},{"title":"Foam Fire-Extinguishing Systems","type":"Proposed Rule","abstract":"The Coast Guard must approve marine foam fire-extinguishing systems. Currently, eight guidance documents set out the existing type approval criteria. The Coast Guard proposes to update and codify the type approval criteria to reflect current industry practices. Criteria updates would reflect advancements in technology, reduce certain testing and design requirements, and reduce the administrative burden on industry and the government. This deregulatory measure would result in cost savings for industry and the government.","document_number":"2026-10413","html_url":"https://www.federalregister.gov/documents/2026/05/26/2026-10413/foam-fire-extinguishing-systems","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-05-26/pdf/2026-10413.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-10413.pdf?1779453919","publication_date":"2026-05-26","agencies":[{"raw_name":"DEPARTMENT OF HOMELAND SECURITY","name":"Homeland Security Department","id":227,"url":"https://www.federalregister.gov/agencies/homeland-security-department","json_url":"https://www.federalregister.gov/api/v1/agencies/227","parent_id":null,"slug":"homeland-security-department"},{"raw_name":"Coast Guard","name":"Coast Guard","id":53,"url":"https://www.federalregister.gov/agencies/coast-guard","json_url":"https://www.federalregister.gov/api/v1/agencies/53","parent_id":227,"slug":"coast-guard"}],"excerpts":"systems <span class=\"match\">must</span> have a water bypass line around the foam proportioner for use when flowing water only. \n \n \n § 162.040-9 \n \n For Coast Guard approval, the tests of this part <span class=\"match\">must</span> be conducted by an independent laboratory. \n \n (a) \n Performance tests. \n Two discharge tests <span class=\"match\">must</span> be conducted for each foam hose reel station for which approval is sought. Each discharge test <span class=\"match\">must</span> be conducted with half of the hose unwound from the foam hose reel station. Each discharge test <span class=\"match\">must</span> <span class=\"match\">include</span>:\n \n \n (i) \n Activation time. \n The foam hose reel station <span class=\"match\">must</span> be capable"},{"title":"Medicare Program; Inpatient Rehabilitation Facility Prospective Payment System for Federal Fiscal Year 2027 and Updates to the IRF Quality Reporting Program","type":"Proposed Rule","abstract":"This proposed rule would update the prospective payment rates for inpatient rehabilitation facilities (IRFs) for Federal fiscal year (FY) 2027. As required by statute, this proposed rule includes the classification and weighting factors for the IRF prospective payment system's case-mix groups and a description of the methodologies and data used in computing the prospective payment rates for FY 2027. It also continues the third year of the 3-year phaseout of the rural adjustment, which began in FY 2025. This proposed rule includes a solicitation for public comments on alternative data sources for the IRF PPS wage index; proposes to require all therapy treatments or therapy evaluations to begin within 36-hours from midnight on the day of admission; proposes to require a patient's current functional status be documented on the preadmission screening; proposes requirements for the initial Interdisciplinary Team meeting; and includes a request for information on potential future IRF PPS payment reform. Additionally, the proposed rule includes updates to the IRF Quality Reporting Program. Furthermore, the proposed rule includes changes to the Durable Medical Equipment, Prosthetics, Orthotics, and Supplies Competitive Bidding Program.","document_number":"2026-06642","html_url":"https://www.federalregister.gov/documents/2026/04/06/2026-06642/medicare-program-inpatient-rehabilitation-facility-prospective-payment-system-for-federal-fiscal","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-04-06/pdf/2026-06642.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-06642.pdf?1775160907","publication_date":"2026-04-06","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"preadmission screening; proposes requirements for the initial Interdisciplinary Team meeting; and <span class=\"match\">includes</span> a request for information on potential future IRF PPS payment reform. Additionally, the proposed rule <span class=\"match\">includes</span> updates to the IRF Quality Reporting Program. Furthermore, the proposed rule <span class=\"match\">includes</span> changes to the Durable Medical Equipment, Prosthetics, Orthotics, and Supplies Competitive Bidding Program. \n \n \n DATES: \n To be assured consideration, comments <span class=\"match\">must</span> be received at one of the addresses provided below by June 1, 2026. \n \n \n ADDRESSES: \n In"},{"title":"Tongass National Forest; Alaska; Land Management Plan Revision","type":"Notice","abstract":"The U.S. Department of Agriculture, Forest Service is revising the land management plan for the Tongass National Forest. This notice announces the Forest Service's initiation of the development of a revised land management plan (revised plan) and intent to prepare an environmental impact statement (EIS) to evaluate the effects of revising the current plan. This notice initiates the scoping period on the development of the proposed action and EIS. This notice also describes the documents and background resources available for review and how to obtain them; includes a description of the preliminary need to change the current land management plan; includes options for meeting the needs for change; includes a preliminary list of substantive issues to be analyzed in detail; provides information on public participation, including the process for submitting comments; provides an estimated schedule for the planning process; and describes how to obtain additional information. The Planning, Administrative Reviews, and Litigation System identification number for the project is 64039.","document_number":"2026-03197","html_url":"https://www.federalregister.gov/documents/2026/02/18/2026-03197/tongass-national-forest-alaska-land-management-plan-revision","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-02-18/pdf/2026-03197.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-03197.pdf?1771335926","publication_date":"2026-02-18","agencies":[{"raw_name":"DEPARTMENT OF AGRICULTURE","name":"Agriculture Department","id":12,"url":"https://www.federalregister.gov/agencies/agriculture-department","json_url":"https://www.federalregister.gov/api/v1/agencies/12","parent_id":null,"slug":"agriculture-department"},{"raw_name":"Forest Service","name":"Forest Service","id":209,"url":"https://www.federalregister.gov/agencies/forest-service","json_url":"https://www.federalregister.gov/api/v1/agencies/209","parent_id":12,"slug":"forest-service"}],"excerpts":"This notice initiates the scoping period on the development of the proposed action and EIS. This notice also describes the documents and background resources available for review and how to obtain them; <span class=\"match\">includes</span> a <span class=\"match\">description</span> of the preliminary need to change the current land management plan; <span class=\"match\">includes</span> options for meeting the needs for change; <span class=\"match\">includes</span> a preliminary list of substantive issues to be analyzed in detail; provides information on public participation, including the process for submitting comments; provides an estimated schedule for the planning"},{"title":"Agricultural Foreign Investment Disclosure Act: Revisions to Reporting Requirements","type":"Proposed Rule","abstract":"The Agricultural Foreign Investment Disclosure Act of 1978 (AFIDA) implementing regulations establish requirements under which foreign persons must report interests in U.S. agricultural lands to the U.S. Department of Agriculture (USDA). AFIDA regulations describe the type of interest in agricultural land a foreign person must have to trigger the reporting requirement, specific information that must be included in the report, and the mechanics of filing the report with USDA. AFIDA also requires some information about foreign persons who hold an interest in the agricultural land even though they may not own it directly, provided those foreign persons have \"significant interest or substantial control\" in the direct interest holder. USDA uses information from the filings to produce periodic reports to Congress on the effect that foreign ownership of U.S. agricultural land has on family farms and rural communities, and for other purposes. AFIDA regulations were last updated in 2006. Since that time, national security attention to foreign ownership or substantial control of agricultural land has increased. Committee on Foreign Investment in the United States (CFIUS) agencies, including the U.S. Department of Defense, use USDA information from AFIDA filings to identify and review transactions that may pose national security risks, such as the location of agricultural land near sensitive military bases. Recent analyses, including a report by the Government Accountability Office (GAO), have identified flaws in USDA's processes for collecting, tracking, and sharing AFIDA data. These deficiencies, combined with evolving national security concerns and a Consolidated Appropriations Act, 2023 requirement for USDA to develop a streamlined process for electronic submission and retention of AFIDA disclosures, lead USDA to examine AFIDA regulations and invite public input on changes that would improve information collection activities in a manner responsive to national security and the use of agricultural land.","document_number":"2025-23830","html_url":"https://www.federalregister.gov/documents/2025/12/29/2025-23830/agricultural-foreign-investment-disclosure-act-revisions-to-reporting-requirements","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-12-29/pdf/2025-23830.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-23830.pdf?1766497514","publication_date":"2025-12-29","agencies":[{"raw_name":"DEPARTMENT OF AGRICULTURE","name":"Agriculture Department","id":12,"url":"https://www.federalregister.gov/agencies/agriculture-department","json_url":"https://www.federalregister.gov/api/v1/agencies/12","parent_id":null,"slug":"agriculture-department"},{"raw_name":"Office of the Secretary"}],"excerpts":"\n The Agricultural Foreign Investment Disclosure Act of 1978 (AFIDA) implementing regulations establish requirements under which foreign persons <span class=\"match\">must</span> report interests in U.S. agricultural lands to the U.S. Department of Agriculture (USDA). AFIDA regulations describe the <span class=\"match\">type</span> of interest in agricultural land a foreign person <span class=\"match\">must</span> have to trigger the reporting requirement, specific information that <span class=\"match\">must</span> be included in the report, and the mechanics of filing the report with USDA. AFIDA also requires some information about foreign persons who hold an"},{"title":"Airworthiness Directives; De Havilland Aircraft of Canada Limited (Type Certificate Previously Held by Bombardier, Inc.) Airplanes","type":"Rule","abstract":"The FAA is adopting a new airworthiness directive (AD) for all De Havilland Aircraft of Canada Limited Model DHC-8 airplanes. This AD was prompted by reports of cracked barrel nuts at the wing front spar and horizontal stabilizer to vertical stabilizer joint. This AD requires repetitive inspections for cracking and corrosion of the affected barrel nuts and applicable corrective actions. The FAA is issuing this AD to address the unsafe condition on these products.","document_number":"2026-11217","html_url":"https://www.federalregister.gov/documents/2026/06/04/2026-11217/airworthiness-directives-de-havilland-aircraft-of-canada-limited-type-certificate-previously-held-by","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-04/pdf/2026-11217.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-11217.pdf?1780490724","publication_date":"2026-06-04","agencies":[{"raw_name":"DEPARTMENT OF TRANSPORTATION","name":"Transportation Department","id":492,"url":"https://www.federalregister.gov/agencies/transportation-department","json_url":"https://www.federalregister.gov/api/v1/agencies/492","parent_id":null,"slug":"transportation-department"},{"raw_name":"Federal Aviation Administration","name":"Federal Aviation Administration","id":159,"url":"https://www.federalregister.gov/agencies/federal-aviation-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/159","parent_id":492,"slug":"federal-aviation-administration"}],"excerpts":"Office.\n \n \n (2) \n Contacting the Manufacturer: \n For any requirement in this AD to obtain instructions from a manufacturer, the instructions <span class=\"match\">must</span> be accomplished using a method approved by the Manager, International Validation Branch, FAA; or Transport Canada; or De Havilland Aircraft of Canada Limited's Transport Canada Design Approval Organization (DAO). If approved by the DAO, the approval <span class=\"match\">must</span> <span class=\"match\">include</span> the DAO-authorized signature.\n \n (j) Additional Information \n \n For more information about this AD, contact Christopher Spencer, Aviation Safety"},{"title":"Notice of Request Under the Freedom of Information Act for Federal Contractors' Type 2 Consolidated EEO-1 Report Data","type":"Notice","abstract":"The U.S. Department of Labor's Office of Federal Contract Compliance Programs (OFCCP) has received two requests under the Freedom of Information Act (FOIA) for 2021 Type 2 Consolidated Employer Information Reports, Standard Form 100 (EEO-1 Report), filed by the federal contractors. These two requests have come from the University of Utah and a non-profit organization named \"As You Sow,\" respectively. OFCCP has reason to believe that the information requested may be protected from disclosure under FOIA Exemption 4, which protects disclosure of confidential commercial information, but has not yet determined whether the requested information is protected from disclosure under that exemption. OFCCP is requesting that entities that filed Type 2 Consolidated EEO-1 Reports as federal contractors for the 2021 reporting year and object to the disclosure of this information submit those objections to OFCCP within 40 days of the date of this Notice.","document_number":"2024-24381","html_url":"https://www.federalregister.gov/documents/2024/10/29/2024-24381/notice-of-request-under-the-freedom-of-information-act-for-federal-contractors-type-2-consolidated","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-10-29/pdf/2024-24381.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-24381.pdf?1730119516","publication_date":"2024-10-29","agencies":[{"raw_name":"DEPARTMENT OF LABOR","name":"Labor Department","id":271,"url":"https://www.federalregister.gov/agencies/labor-department","json_url":"https://www.federalregister.gov/api/v1/agencies/271","parent_id":null,"slug":"labor-department"},{"raw_name":"Office of Federal Contract Compliance Programs","name":"Federal Contract Compliance Programs Office","id":162,"url":"https://www.federalregister.gov/agencies/federal-contract-compliance-programs-office","json_url":"https://www.federalregister.gov/api/v1/agencies/162","parent_id":271,"slug":"federal-contract-compliance-programs-office"}],"excerpts":"If you are deaf, hard of hearing, or have a speech disability, please dial 7-1-1 to access telecommunications relay services. \n \n \n \n SUPPLEMENTARY INFORMATION: \n \n Background \n A. Background on EEO-1 Reports \n Multi-establishment employers <span class=\"match\">must</span> file annually a “Consolidated Report” (formerly known as a <span class=\"match\">Type</span> 2 Report) for all employees at the employer's headquarters as well as all its establishments, categorized by job category, sex, and race or ethnicity. \n \n Since 1966, the Equal Employment Opportunity Commission (EEOC) has required eligible employers"},{"title":"Medicare Program; Inpatient Rehabilitation Facility Prospective Payment System for Federal Fiscal Year 2026 and Updates to the IRF Quality Reporting Program","type":"Rule","abstract":"This final rule updates the prospective payment rates for inpatient rehabilitation facilities (IRFs) for Federal fiscal year (FY) 2026. As required by statute, this final rule includes the classification and weighting factors for the IRF prospective payment system's case-mix groups and a description of the methodologies and data used in computing the prospective payment rates for FY 2026. It also continues the second year of the 3-year phaseout of the rural adjustment, which began in FY 2025. Additionally, the final rule includes updates to the IRF Quality Reporting Program.","document_number":"2025-14780","html_url":"https://www.federalregister.gov/documents/2025/08/05/2025-14780/medicare-program-inpatient-rehabilitation-facility-prospective-payment-system-for-federal-fiscal","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-08-05/pdf/2025-14780.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-14780.pdf?1754079306","publication_date":"2025-08-05","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"accordance with the Medicare Claims Processing Manual, chapter 3, section 20.3 (Pub. 100-04), hospitals (including IRFs) <span class=\"match\">must</span> submit to their MAC an informational-only bill (<span class=\"match\">type</span> of bill (TOB) 111) that <span class=\"match\">includes</span> Condition Code 04. This will ensure that the MA days are included in the hospital's Supplemental Security Income (SSI) ratio (used in calculating the IRF LIP adjustment) for FY 2007 and beyond. Claims submitted to Medicare <span class=\"match\">must</span> comply with- both ASCA and HIPAA. \n \n Section 3 of the ASCA amended section 1862(a) of the Act by adding paragraph (22)"},{"title":"Medical Devices; Immunology and Microbiology Devices; Classification of the SARS-CoV-2 Serology Test","type":"Rule","abstract":"The Food and Drug Administration (FDA) is classifying the SARS-CoV-2 serology test into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the SARS- CoV-2 serology test. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.","document_number":"2026-12902","html_url":"https://www.federalregister.gov/documents/2026/06/26/2026-12902/medical-devices-immunology-and-microbiology-devices-classification-of-the-sars-cov-2-serology-test","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-26/pdf/2026-12902.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-12902.pdf?1782391512","publication_date":"2026-06-26","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"specimen <span class=\"match\">types</span> claimed by this device; alternatively, the sample collection device <span class=\"match\">must</span> be cleared in a premarket submission as a part of this device. \n (3) The labeling required under § 809.10(b) of this chapter <span class=\"match\">must</span> <span class=\"match\">include</span>: \n (i) A <span class=\"match\">detailed</span> device <span class=\"match\">description</span>, including reagents, instruments, ancillary materials, all control elements, and a <span class=\"match\">detailed</span> explanation of the methodology, including all pre-analytical methods for processing of specimens; \n (ii) <span class=\"match\">Detailed</span> <span class=\"match\">descriptions</span> of the performance characteristics of the device for each specimen <span class=\"match\">type</span> claimed"},{"title":"Unaccompanied Children Program Foundational Rule; Sponsor Assessment Update To Include Proof of Identity, Background Check, Placement, and Income Verification Standards","type":"Proposed Rule","abstract":"This notice of proposed rulemaking (NPRM, or proposed rule) would establish certain additional requirements for sponsor suitability assessments related to proof of identity, proof of income, and other information required for background checks to promote the safe placement of unaccompanied alien children (UAC). This NPRM proposes acceptable documentation for proof of identity and would require proof of income from potential sponsors of UAC in ORR custody by reason of their immigration status, as described in the Homeland Security Act of 2002 (HSA) and the William Wilberforce Trafficking Victims Protection Reauthorization Act of 2008 (TVPRA). This NPRM also proposes amendments to background check requirements for sponsor suitability assessments and the conduct of examinations of UAC related to considerations of UAC dangerousness to self or others that align with the One Big Beautiful Bill Act. Finally, this NPRM proposes certain administrative updates to align numbering and terminology between proposals and existing regulations. The docket on https://www.regulations.gov will include a plain language summary of the NPRM.","document_number":"2026-12946","html_url":"https://www.federalregister.gov/documents/2026/06/26/2026-12946/unaccompanied-children-program-foundational-rule-sponsor-assessment-update-to-include-proof-of","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-26/pdf/2026-12946.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-12946.pdf?1782391518","publication_date":"2026-06-26","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Administration for Children and Families","name":"Children and Families Administration","id":49,"url":"https://www.federalregister.gov/agencies/children-and-families-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/49","parent_id":221,"slug":"children-and-families-administration"}],"excerpts":"RIN 0970-AD26 in the subject line of the message.\n \n \n Instructions: \n All submissions received <span class=\"match\">must</span> <span class=\"match\">include</span> the agency name and docket number or RIN for this rulemaking. For <span class=\"match\">detailed</span> instructions on submitting comments and additional information on the rulemaking process, see the “Public Participation” heading of the \n SUPPLEMENTARY INFORMATION \n section of this document.\n \n \n \n FOR FURTHER INFORMATION CONTACT: \n \n Toby Biswas, Assistant Deputy Director-Policy, Unaccompanied Alien Children Bureau, Office of Refugee Resettlement, Administration for"},{"title":"Endangered and Threatened Wildlife and Plants; Review of Species That Are Candidates for Listing as Endangered or Threatened; Annual Notification of Findings on Resubmitted Petitions; Annual Description of Progress on Listing Actions","type":"Proposed Rule","abstract":"In this candidate notice of review (CNOR), we, the U.S. Fish and Wildlife Service (Service or FWS), present an updated list of plant and animal species that we regard as candidates for or have proposed for addition to the Lists of Endangered and Threatened Wildlife and Plants under the Endangered Species Act of 1973, as amended. This document also includes our findings on resubmitted petitions and describes our progress in revising the Lists of Endangered and Threatened Wildlife and Plants (Lists) during the period October 1, 2022, through September 30, 2024. Combined with other decisions for individual species that were published separately from this CNOR in the past two years, the current number of species that are candidates for listing or uplisting is 16 (as of September 30, 2024). Identification of candidate species can assist environmental planning efforts by providing advance notice of potential listings, and by allowing landowners, resource managers, States, Tribes, range countries, and other stakeholders to take actions to alleviate threats and thereby possibly remove the need to list species as endangered or threatened. Even if we subsequently list a candidate species, the early notice provided here could result in more options for species management and recovery by prompting earlier candidate conservation measures to alleviate threats to the species.","document_number":"2025-19732","html_url":"https://www.federalregister.gov/documents/2025/10/31/2025-19732/endangered-and-threatened-wildlife-and-plants-review-of-species-that-are-candidates-for-listing-as","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-10-31/pdf/2025-19732.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-19732.pdf?1761828308","publication_date":"2025-10-31","agencies":[{"raw_name":"DEPARTMENT OF THE INTERIOR","name":"Interior Department","id":253,"url":"https://www.federalregister.gov/agencies/interior-department","json_url":"https://www.federalregister.gov/api/v1/agencies/253","parent_id":null,"slug":"interior-department"},{"raw_name":"Fish and Wildlife Service","name":"Fish and Wildlife Service","id":197,"url":"https://www.federalregister.gov/agencies/fish-and-wildlife-service","json_url":"https://www.federalregister.gov/api/v1/agencies/197","parent_id":253,"slug":"fish-and-wildlife-service"}],"excerpts":"instances. Under section 4(b)(3)(A) of the Act, when we receive a petition to list a species, we <span class=\"match\">must</span> determine within 90 days, to the maximum extent practicable, whether the petition presents substantial information indicating that listing may be warranted (a “90-day finding”). If we make a positive 90-day finding, we <span class=\"match\">must</span> promptly commence a status review of the species under section 4(b)(3)(A), and then, in accordance with section 4(b)(3)(B), we <span class=\"match\">must</span> make, within 12 months of the receipt of the petition, one of the following three possible findings"},{"title":"Medical Devices; Immunology and Microbiology Devices; Classification of the Spinal Muscular Atrophy Newborn Screening Test System","type":"Rule","abstract":"The Food and Drug Administration (FDA) is classifying the Spinal Muscular Atrophy newborn screening test system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the Spinal Muscular Atrophy newborn screening test system. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.","document_number":"2026-11740","html_url":"https://www.federalregister.gov/documents/2026/06/11/2026-11740/medical-devices-immunology-and-microbiology-devices-classification-of-the-spinal-muscular-atrophy","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-11/pdf/2026-11740.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-11740.pdf?1781095520","publication_date":"2026-06-11","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"or provided. The <span class=\"match\">description</span> <span class=\"match\">must</span> identify those control elements that are incorporated into the testing procedure. \n (iv) <span class=\"match\">Detailed</span> specifications for the filter paper to be used as part of the device, which <span class=\"match\">must</span> be appropriately labeled for in vitro diagnostic use. Specifications <span class=\"match\">must</span> <span class=\"match\">include</span> punch size and address any properties of the filter paper that may interfere with obtaining test results. \n (v) <span class=\"match\">Detailed</span> documentation of the following analytical and clinical studies, including the study protocols containing <span class=\"match\">descriptions</span> of the test methods"},{"title":"Medical Devices; Immunology and Microbiology Devices; Classification of the Simple In Vitro Diagnostic Device for the Detection of Secreted Proteins From Bacillus Species (spp.) in Human Clinical Samples","type":"Rule","abstract":"The Food and Drug Administration (FDA) is classifying the simple in vitro diagnostic device for the detection of secreted proteins from Bacillus species (spp.) in human clinical samples into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the simple in vitro diagnostic device for the detection of secreted proteins from Bacillus species (spp.) in human clinical samples. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.","document_number":"2026-12443","html_url":"https://www.federalregister.gov/documents/2026/06/22/2026-12443/medical-devices-immunology-and-microbiology-devices-classification-of-the-simple-in-vitro-diagnostic","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-22/pdf/2026-12443.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-12443.pdf?1781786720","publication_date":"2026-06-22","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"appropriate. This study <span class=\"match\">must</span> <span class=\"match\">include</span> prospective (sequentially collected) samples for each intended sample <span class=\"match\">type</span> that are representative of the intended use populations and may, when determined to be acceptable by FDA, <span class=\"match\">include</span> additional characterized clinical samples; or, as an alternative, when determined to be acceptable by FDA, an equivalent sample set. This study <span class=\"match\">must</span> <span class=\"match\">include</span> samples spanning all relevant analyte concentrations for all of the indicated sample <span class=\"match\">type</span>(s) and the targeted analyte(s). \n (iv) A <span class=\"match\">detailed</span> <span class=\"match\">description</span> of the impact of any"},{"title":"Medical Devices; Immunology and Microbiology Devices; Classification of the Simple Point-of-Care Device to Directly Detect SARS-CoV-2 Viral Targets From Clinical Specimens in Near-Patient Settings","type":"Rule","abstract":"The Food and Drug Administration (FDA) is classifying the simple point-of-care device to directly detect SARS-CoV-2 viral targets from clinical specimens in near-patient settings into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the simple point-of-care device to directly detect SARS-CoV-2 viral targets from clinical specimens in near-patient settings. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.","document_number":"2026-11739","html_url":"https://www.federalregister.gov/documents/2026/06/11/2026-11739/medical-devices-immunology-and-microbiology-devices-classification-of-the-simple-point-of-care","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-11/pdf/2026-11739.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-11739.pdf?1781095520","publication_date":"2026-06-11","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"(A) This documentation <span class=\"match\">must</span> <span class=\"match\">include</span> a <span class=\"match\">detailed</span> <span class=\"match\">description</span> of a protocol (including all procedures and methods) for the continuous monitoring, identification, and handling of genetic mutations and/or novel isolates or strains (\n e.g., \n regular review of published literature and periodic in silico analysis of target sequences to detect possible mismatches). Protocols <span class=\"match\">must</span> <span class=\"match\">include</span> plans to update labeling with additional performance data. All results of this protocol, including any findings, <span class=\"match\">must</span> be documented and <span class=\"match\">must</span> <span class=\"match\">include</span> any additional data analysis"},{"title":"Commercial Leasing for Outer Continental Shelf Minerals Offshore Alaska-Request for Information and Interest","type":"Notice","abstract":"The Bureau of Ocean Energy Management (BOEM) is initiating the first steps that could potentially lead to a lease sale for minerals on the Outer Continental Shelf (OCS) offshore Alaska by publishing this request for information and interest (RFI). This RFI is not a final decision to lease and does not prejudge any future Secretarial decisions concerning leasing on the OCS offshore Alaska. This RFI requests information and comments on, and indications of interest in, the leasing of OCS minerals in an area offshore Alaska, referred to as the RFI Area, with details in Section 5 \"Description of the RFI Area.\" BOEM will consider information and interest received in response to this RFI when considering whether to proceed with additional steps leading to the offer of OCS minerals for lease offshore Alaska. Those interested in providing comments or information should provide the information requested in Section 6 \"Types of Information and Comments Requested,\" of this RFI. Those interested in leasing in and around the RFI Area for OCS mineral development should provide the information described in Section 7 \"Requested Information for Indications of Interest.\" BOEM will decide whether and under what terms and conditions to hold a lease sale for commercial OCS mineral development offshore Alaska after further consideration, consultations, public participation, and environmental analyses.","document_number":"2026-01808","html_url":"https://www.federalregister.gov/documents/2026/01/29/2026-01808/commercial-leasing-for-outer-continental-shelf-minerals-offshore-alaska-request-for-information-and","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-01-29/pdf/2026-01808.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-01808.pdf?1769607919","publication_date":"2026-01-29","agencies":[{"raw_name":"DEPARTMENT OF THE INTERIOR","name":"Interior Department","id":253,"url":"https://www.federalregister.gov/agencies/interior-department","json_url":"https://www.federalregister.gov/api/v1/agencies/253","parent_id":null,"slug":"interior-department"},{"raw_name":"Bureau of Ocean Energy Management","name":"Ocean Energy Management Bureau","id":575,"url":"https://www.federalregister.gov/agencies/ocean-energy-management-bureau","json_url":"https://www.federalregister.gov/api/v1/agencies/575","parent_id":253,"slug":"ocean-energy-management-bureau"}],"excerpts":"fisheries, including but not limited to, the use of the areas, the fishing gear <span class=\"match\">types</span> used, seasonal use, and recommendations for reducing use conflicts. \n f. Relative environmental sensitivity and marine productivity in and around the RFI Area. \n g. Information on the preliminary activities necessary to develop comprehensive delineation, testing, or mining plans, particularly the <span class=\"match\">types</span> of any necessary surveys and associated equipment. \n h. Information on the <span class=\"match\">types</span> of activities associated with delineation, testing, or mining of OCS minerals. "},{"title":"Medicare Program; Inpatient Rehabilitation Facility Prospective Payment System for Federal Fiscal Year 2026 and Updates to the IRF Quality Reporting Program","type":"Proposed Rule","abstract":"This proposed rule would update the prospective payment rates for inpatient rehabilitation facilities (IRFs) for Federal fiscal year (FY) 2026. As required by statute, this proposed rule includes the proposed classification and weighting factors for the IRF prospective payment system's case-mix groups and a description of the methodologies and data used in computing the prospective payment rates for FY 2026. It also continues the second year of the 3-year phaseout of the rural adjustment, which began in FY 2025. Additionally, the proposed rule includes updates to the IRF Quality Reporting Program (QRP).","document_number":"2025-06336","html_url":"https://www.federalregister.gov/documents/2025/04/30/2025-06336/medicare-program-inpatient-rehabilitation-facility-prospective-payment-system-for-federal-fiscal","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-04-30/pdf/2025-06336.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-06336.pdf?1744402509","publication_date":"2025-04-30","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"required by statute, this proposed rule <span class=\"match\">includes</span> the proposed classification and weighting factors for the IRF prospective payment system's case-mix groups and a <span class=\"match\">description</span> of the methodologies and data used in computing the prospective payment rates for FY 2026. It also continues the second year of the 3-year phaseout of the rural adjustment, which began in FY 2025. Additionally, the proposed rule <span class=\"match\">includes</span> updates to the IRF Quality Reporting Program (QRP). \n \n \n DATES: \n To be assured consideration, comments <span class=\"match\">must</span> be received at one of the addresses"},{"title":"Natural Resource Damages for Hazardous Substances","type":"Rule","abstract":"This final rule revises the simplified Type A procedures in the regulations for conducting natural resource damage assessments for hazardous substance releases. Additionally, this final rule includes several conforming changes and corrections intended to fix citations, provide for consistent use of terminology, and remove outdated or duplicative rule provisions and definitions. The Department of the Interior (Interior) is removing provisions that it believes are no longer applicable, clarifying other provisions by incorporating language that would implement existing Interior regulatory interpretations, and making other changes and corrections. These revisions also allow for the regulations to meet information collection requirements mandated by the Office of Management and Budget.","document_number":"2026-14052","html_url":"https://www.federalregister.gov/documents/2026/07/13/2026-14052/natural-resource-damages-for-hazardous-substances","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-07-13/pdf/2026-14052.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-14052.pdf?1783687515","publication_date":"2026-07-13","agencies":[{"raw_name":"DEPARTMENT OF THE INTERIOR","name":"Interior Department","id":253,"url":"https://www.federalregister.gov/agencies/interior-department","json_url":"https://www.federalregister.gov/api/v1/agencies/253","parent_id":null,"slug":"interior-department"},{"raw_name":"Office of the Secretary"}],"excerpts":"the ICs in this rule as follows:\n \n \n (1) \n <span class=\"match\">Type</span> A Report (Existing/Modified) \n —If a <span class=\"match\">Type</span> A procedure is used, the report already <span class=\"match\">must</span> <span class=\"match\">include</span> the information specified in subpart D (43 CFR 11.90(b)). This rulemaking seeks to clarify the content of the <span class=\"match\">Type</span> A report based on the proposed changes in the sections itemized below. The <span class=\"match\">Type</span> A report <span class=\"match\">must</span> be made available to the public and provide for a comment period of at least 30 days.\n \n \n Information collected in a <span class=\"match\">Type</span> A Report <span class=\"match\">includes</span>: \n \n (a) The <span class=\"match\">Type</span> A Report is a document to provide the public"},{"title":"Medical Devices; Radiology Devices; Classification of the Radiological Machine Learning-Based Quantitative Imaging Software With Predetermined Change Control Plan","type":"Rule","abstract":"The Food and Drug Administration (FDA) is classifying the radiological machine learning-based quantitative imaging software with predetermined change control plan into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the radiological machine learning-based quantitative imaging software with predetermined change control plan. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.","document_number":"2026-12166","html_url":"https://www.federalregister.gov/documents/2026/06/17/2026-12166/medical-devices-radiology-devices-classification-of-the-radiological-machine-learning-based","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-17/pdf/2026-12166.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-12166.pdf?1781613912","publication_date":"2026-06-17","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"imaging outputs. The device <span class=\"match\">includes</span> functions to support outputs such as view selection, segmentation and landmarking. The design specifications <span class=\"match\">include</span> planned modifications that may be made to the device consistent with an established predetermined change control plan.\n \n \n (b) \n Classification. \n Class II (special controls). The special controls for this device are:\n \n (1) Design verification and validation <span class=\"match\">must</span> <span class=\"match\">include</span>: \n (i) A <span class=\"match\">detailed</span> <span class=\"match\">description</span> of the image postprocessing algorithms, including a <span class=\"match\">detailed</span> <span class=\"match\">description</span> of the algorithm inputs"}]}