documents: FDA-2022-N-0150-0017

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0150-0017 FDA FDA-2022-N-0150 Revocation of Authorization of Emergency Use of In Vitro Diagnostic Device for Detection and/or Diagnosis of COVID–19; Availability Notice Announcement 2025-08-15T04:00:00Z 2025 8 2025-08-15T04:00:00Z   2025-08-15T17:38:51Z 2025-15556 0 0 09000064b8f00dc5

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