{"description":"Documents matching 'sunlamp' and published on or after 01/01/2025","count":3,"total_pages":1,"results":[{"title":"General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use of Sunlamp Products; Withdrawal of Proposed Rule","type":"Proposed Rule","abstract":"The Food and Drug Administration (FDA) is announcing the withdrawal of the proposed rule titled \"General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use of Sunlamp Products,\" which published in the Federal Register of December 22, 2015. FDA is taking this action because it no longer intends to finalize the proposed rule.","document_number":"2026-05103","html_url":"https://www.federalregister.gov/documents/2026/03/16/2026-05103/general-and-plastic-surgery-devices-restricted-sale-distribution-and-use-of-sunlamp-products","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-03-16/pdf/2026-05103.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-05103.pdf?1773405919","publication_date":"2026-03-16","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":"20(b)(9) (21 CFR 878.4635(a) and 1040.20(b)(9))). <span class=\"match\">Sunlamp</span> products include tanning beds and tanning booths. <span class=\"match\">Sunlamp</span> products as defined in the Proposed Rule did not include ultraviolet lamps for dermatological disorders regulated under 21 CFR 878.4630.\n \n FDA has undertaken several regulatory initiatives related to <span class=\"match\">sunlamp</span> products. Previously, in a final reclassification order that we issued on June 2, 2014 (79 FR 31205), FDA reclassified <span class=\"match\">sunlamp</span> products and UV lamps intended for use in <span class=\"match\">sunlamp</span> products from class I to class II, making them subject"},{"title":"Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Electronic Products Requirements","type":"Notice","abstract":"The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.","document_number":"2026-03097","html_url":"https://www.federalregister.gov/documents/2026/02/18/2026-03097/agency-information-collection-activities-submission-for-office-of-management-and-budget-review","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-02-18/pdf/2026-03097.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-03097.pdf?1771335911","publication_date":"2026-02-18","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":"• Form FDA 3628 “General Annual Report (Includes Medical, Analytical, and Industrial X-Ray Products Annual Report)” \n • Form FDA 3629 “Abbreviated Report” \n • Form FDA 3630 “Guide for Preparing Product Reports on <span class=\"match\">Sunlamps</span> and <span class=\"match\">Sunlamp</span> Products” \n • Form FDA 3631 “Guide for Preparing Annual Reports on Radiation Safety Testing of <span class=\"match\">Sunlamp</span> Products” \n • Form FDA 3632 “Guide for Preparing Product Reports on Lasers and Products Containing Lasers” \n • Form FDA 3633 “General Variance Request” \n • Form FDA 3634 “Television Products Annual Report” \n • Form"},{"title":"Agency Information Collection Activities; Proposed Collection; Comment Request; Electronic Products","type":"Notice","abstract":"The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on requirements for reporting and recordkeeping, general and specific requirements, and the availability of sample electronic products for manufacturers and distributors of electronic products.","document_number":"2025-13052","html_url":"https://www.federalregister.gov/documents/2025/07/14/2025-13052/agency-information-collection-activities-proposed-collection-comment-request-electronic-products","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-07-14/pdf/2025-13052.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-13052.pdf?1752237910","publication_date":"2025-07-14","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":"• Form FDA 3628 “General Annual Report (Includes Medical, Analytical, and Industrial X-Ray Products Annual Report)” \n • Form FDA 3629 “Abbreviated Report” \n • Form FDA 3630 “Guide for Preparing Product Reports on <span class=\"match\">Sunlamps</span> and <span class=\"match\">Sunlamp</span> Products” \n • Form FDA 3631 “Guide for Preparing Annual Reports on Radiation Safety Testing of <span class=\"match\">Sunlamp</span> Products” \n • Form FDA 3632 “Guide for Preparing Product Reports on Lasers and Products Containing Lasers” \n • Form FDA 3633 “General Variance Request” \n • Form FDA 3634 “Television Products Annual Report” \n • Form"}]}