{"abstract":"The Food and Drug Administration (FDA) is amending certain medical device regulations to correct typographical errors and to ensure accuracy and clarity in the agency's regulations.","action":"Final rule; technical amendment.","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/2007/04/09/E7-6290.html","cfr_references":[{"chapter":null,"citation_url":null,"part":803,"title":21},{"chapter":null,"citation_url":null,"part":814,"title":21},{"chapter":null,"citation_url":null,"part":820,"title":21},{"chapter":null,"citation_url":null,"part":821,"title":21},{"chapter":null,"citation_url":null,"part":822,"title":21},{"chapter":null,"citation_url":null,"part":874,"title":21},{"chapter":null,"citation_url":null,"part":886,"title":21},{"chapter":null,"citation_url":null,"part":1002,"title":21},{"chapter":null,"citation_url":null,"part":1005,"title":21},{"chapter":null,"citation_url":null,"part":1020,"title":21}],"citation":"72 FR 17397","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"April 9, 2007.","disposition_notes":null,"docket_ids":["Docket No. 2007N-0104"],"dockets":[{"supporting_documents":[],"agency_name":"FDA","documents":[{"comment_count":null,"comment_start_date":null,"updated_at":"2025-07-15T14:56:17.534-04:00","comment_url":"https://www.regulations.gov/commenton/FDA-2007-N-0091-0001","allow_late_comments":false,"id":"FDA-2007-N-0091-0001","comment_end_date":null,"regulations_dot_gov_open_for_comment":false}],"supporting_documents_count":0,"id":"FDA-2007-N-0091","title":"Medical Devices; Technical Amendment - CLOSED"}],"document_number":"E7-6290","effective_on":null,"end_page":17401,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2007/04/09/E7-6290.xml","html_url":"https://www.federalregister.gov/documents/2007/04/09/E7-6290/medical-devices-technical-amendment","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/E7-6290?publication_date=2007-04-09","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2007-04-09/E7-6290/mods.xml","not_received_for_publication":null,"page_length":5,"page_views":{"count":515,"last_updated":"2026-08-24 04:15:06 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2007-04-09/pdf/E7-6290.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"2007-04-09","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2007/04/09/E7-6290.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-2007-N-0091","supporting_documents_count":0,"docket_id":"FDA-2007-N-0091","document_id":"FDA-2007-N-0091-0001","regulation_id_number":null,"title":"Medical Devices; Technical Amendment - CLOSED","checked_regulationsdotgov_at":"2025-07-16T20:55:03Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":17397,"subtype":null,"title":"Medical Devices; Technical Amendment","toc_doc":"Technical amendments","toc_subject":"Medical devices:","topics":["Administrative practice and procedure","Confidential business information","Electronic products","Imports","Medical devices","Medical research","Ophthalmic goods and services","Radiation protection","Reporting and recordkeeping requirements","Surety bonds","Television","X-rays"],"type":"Rule","volume":72}