{"abstract":"The Food and Drug Administration (FDA, the Agency, or we) is amending certain medical device regulations to update a citation for information collection and conform the regulatory provisions to the Federal Food, Drug, and Cosmetics Act (FD&C Act). The rule does not impose any new requirements on affected parties. This action is editorial in nature to correct errors and to ensure accuracy and clarity in the Agency's regulations.","action":"Final rule; technical amendments.","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"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2024/03/15/2024-05473.html","cfr_references":[{"chapter":null,"citation_url":null,"part":807,"title":21},{"chapter":null,"citation_url":null,"part":814,"title":21}],"citation":"89 FR 18792","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"This rule is March 15, 2024.","disposition_notes":null,"docket_ids":["Docket No. FDA-2024-N-1052"],"dockets":[{"supporting_documents":[],"agency_name":"FDA","documents":[{"comment_count":0,"comment_start_date":"2024-03-15","updated_at":"2024-09-03T16:47:43.110-04:00","comment_url":"https://www.regulations.gov/commenton/FDA-2024-N-1052-0001","allow_late_comments":false,"id":"FDA-2024-N-1052-0001","comment_end_date":null,"regulations_dot_gov_open_for_comment":false}],"supporting_documents_count":0,"id":"FDA-2024-N-1052","title":"Medical Devices; Technical Amendments"}],"document_number":"2024-05473","effective_on":null,"end_page":18793,"executive_order_notes":null,"executive_order_number":null,"explanation":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2024/03/15/2024-05473.xml","html_url":"https://www.federalregister.gov/documents/2024/03/15/2024-05473/medical-devices-technical-amendments","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2024-05473?publication_date=2024-03-15","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2024-03-15/2024-05473/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":1860,"last_updated":"2026-04-04 12:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-03-15/pdf/2024-05473.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-05473.pdf?1710420320","publication_date":"2024-03-15","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2024/03/15/2024-05473.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[],"comments_count":0,"agency_id":"FDA","comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2024-N-1052","supporting_documents_count":0,"docket_id":"FDA-2024-N-1052","document_id":"FDA-2024-N-1052-0001","regulation_id_number":null,"title":"Medical Devices; Technical Amendments","checked_regulationsdotgov_at":"2024-03-16T14:00:07Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":18792,"subtype":null,"title":"Medical Devices; Technical Amendments","toc_doc":"Medical Devices; Technical Amendments","toc_subject":null,"topics":["Administrative practice and procedure","Confidential business information","Imports","Medical devices","Medical research","Reporting and recordkeeping requirements"],"type":"Rule","volume":89}