{"abstract":"The Food and Drug Administration (FDA) is amending its regulations for petitioning for device reclassification to update mailing addresses for the petitions. This action is being taken to improve the accuracy of the 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/2014/12/24/2014-30141.html","cfr_references":[{"chapter":null,"citation_url":null,"part":860,"title":21}],"citation":"79 FR 77387","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"This rule is effective December 24, 2014.","disposition_notes":null,"docket_ids":["Docket No. FDA-2013-N-1529"],"dockets":[],"document_number":"2014-30141","effective_on":"2014-12-24","end_page":77388,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2014/12/24/2014-30141.xml","html_url":"https://www.federalregister.gov/documents/2014/12/24/2014-30141/medical-device-classification-procedures-reclassification-petition-content-and-form-technical","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2014-30141?publication_date=2014-12-24","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2014-12-24/2014-30141/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":467,"last_updated":"2026-10-25 08:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2014-12-24/pdf/2014-30141.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2014-30141.pdf?1419342636","publication_date":"2014-12-24","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2014/12/24/2014-30141.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[{"title":"Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals","document_id":"FDA-2013-N-1529-0029"},{"title":"Agency Information Collection\nActivities; Submission for Office of\nManagement and Budget Review;\nComment Request; Reclassification\nPetitions for Medical Devices","document_id":"FDA-2013-N-1529-0027"},{"title":"Agency Information Collection\nActivities; Submission for Office of\nManagement and Budget Review;\nComment Request; Reclassification\nPetitions for Medical Devices","document_id":"FDA-2013-N-1529-0026"},{"title":"Agency Information Collection Activities; Proposed Collection; Comment Request; Reclassification Petitions for Medical Devices","document_id":"FDA-2013-N-1529-0025"},{"title":"04 Reference 3 Final Regulatory Impact Analysis - Medical Device Classification Procedures: Incorporating FDA Safety and Innovation Act Procedures","document_id":"FDA-2013-N-1529-0024"},{"title":"03 Reference 2 Open Public Hearings Guidance - Guidance for the Public, FDA Advisory Committee Members, and FDA Staff: The Open Public Hearing at FDA Advisory Committee Meetings","document_id":"FDA-2013-N-1529-0023"},{"title":"02 Reference 1 Medical Device Classification Product Codes Guidance for Industry","document_id":"FDA-2013-N-1529-0022"},{"title":"01 Index to References - Final Rule, Medical Device Classification Procedures: Incorporating FDA Safety and Innovation Act Procedures","document_id":"FDA-2013-N-1529-0021"},{"title":"Medical Device Classification Procedures: Incorporating Food and\nDrug Administration Safety and Innovation Act Procedures","document_id":"FDA-2013-N-1529-0020"},{"title":"Medical Device Classification Procedures; Change of Address; Technical Amendment","document_id":"FDA-2013-N-1529-0019"}],"comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2013-N-1529","supporting_documents_count":13,"docket_id":"FDA-2013-N-1529","regulation_id_number":null,"title":"Medical Device Classification Procedures","checked_regulationsdotgov_at":"2015-01-13T06:00:18Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":77387,"subtype":null,"title":"Medical Device Classification Procedures; Reclassification Petition: Content and Form; Technical Amendment","toc_doc":"Reclassification Petition: Content and Form; Technical Amendment","toc_subject":"Medical Device Classification Procedures:","topics":["Administrative practice and procedure","Medical devices"],"type":"Rule","volume":79}