{"abstract":"The Food and Drug Administration (FDA or Agency) is announcing the withdrawal of the guidance document entitled \"Effects of the COVID-19 Public Health Emergency on Formal Meetings and User Fee Applications for Medical Devices--Questions and Answers (Revised),\" which was issued in June 2020 (and updated December 2020). FDA is withdrawing this guidance document in recognition that the conditions that created the need for these policies have evolved, such that these policies are no longer needed.","action":"Notice; withdrawal.","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/2022/06/07/2022-12176.html","cfr_references":[],"citation":"87 FR 34691","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"The withdrawal date is July 7, 2022.","disposition_notes":null,"docket_ids":["Docket No. FDA-2020-D-1138"],"dockets":[],"document_number":"2022-12176","effective_on":null,"end_page":34692,"executive_order_notes":null,"executive_order_number":null,"explanation":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2022/06/07/2022-12176.xml","html_url":"https://www.federalregister.gov/documents/2022/06/07/2022-12176/effects-of-the-covid-19-public-health-emergency-on-formal-meetings-and-user-fee-applications-for","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2022-12176?publication_date=2022-06-07","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2022-06-07/2022-12176/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":2449,"last_updated":"2026-04-04 14:15:05 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2022-06-07/pdf/2022-12176.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2022-12176.pdf?1654260330","publication_date":"2022-06-07","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2022/06/07/2022-12176.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-2020-D-1138","supporting_documents_count":0,"docket_id":"FDA-2020-D-1138","document_id":"FDA-2020-D-1138-0153","regulation_id_number":null,"title":"Center for Devices and Radiological Health (CDRH):  COVID-19","checked_regulationsdotgov_at":"2022-06-08T03:30:05Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":34691,"subtype":null,"title":"Effects of the COVID-19 Public Health Emergency on Formal Meetings and User Fee Applications for Medical Devices-Questions and Answers (Revised); Withdrawal of Guidance","toc_doc":"Effects of the COVID19 Public Health Emergency on Formal Meetings and User Fee Applications for Medical Devices: Questions and Answers; Withdrawal","toc_subject":"Guidance:\n","topics":[],"type":"Notice","volume":87}