documents: FDA-2022-N-0150-0013

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2022-N-0150-0013 FDA FDA-2022-N-0150 Revocation of Two Authorizations of Emergency Use of In Vitro Diagnostic Devices for Detection and/or Diagnosis of COVID–19; Availability Notice Announcement 2024-11-20T05:00:00Z 2024 11 2024-11-20T05:00:00Z   2024-11-20T14:49:41Z 2024-27094 0 0 0900006486829fe4

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