documents: FDA-2022-N-0150-0005

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0150-0005 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 General Notice 2022-06-27T04:00:00Z 2022 6 2022-06-27T04:00:00Z   2022-06-27T13:19:48Z 2022-13639 0 0 090000648519eff7

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