{"abstract":"The Food and Drug Administration (FDA or Agency) is amending the Medical Device Classification Procedures regulation to reflect a change in address for the Center for Devices and Radiological Health (CDRH). This action is editorial in nature and is intended to improve the accuracy of 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/2017/08/21/2017-17564.html","cfr_references":[{"chapter":null,"citation_url":null,"part":860,"title":21}],"citation":"82 FR 39534","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"This rule is effective August 21, 2017<INF>.</INF>","disposition_notes":null,"docket_ids":["Docket No. FDA-2013-N-1529"],"dockets":[],"document_number":"2017-17564","effective_on":"2017-08-21","end_page":39535,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2017/08/21/2017-17564.xml","html_url":"https://www.federalregister.gov/documents/2017/08/21/2017-17564/medical-device-classification-procedures-change-of-address-technical-amendment","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2017-17564?publication_date=2017-08-21","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2017-08-21/2017-17564/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":349,"last_updated":"2026-10-22 20:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2017-08-21/pdf/2017-17564.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2017-17564.pdf?1503060359","publication_date":"2017-08-21","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2017/08/21/2017-17564.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":"2017-09-10T06:00:19Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":39534,"subtype":null,"title":"Medical Device Classification Procedures; Change of Address; Technical Amendment","toc_doc":"Medical Device Classification Procedures; Change of Address; Technical Amendment","toc_subject":null,"topics":["Administrative practice and procedure","Medical devices"],"type":"Rule","volume":82}