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withdrawn,object_id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
FDA-2022-N-0150-0012,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,General Notice,2024-09-03T04:00:00Z,2024,9,,,2024-09-03T13:45:28Z,2024-19724,0,0,09000064866bd595
FDA-2022-N-0150-0011,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,2024-07-25T04:00:00Z,2024,7,2024-07-25T04:00:00Z,,2024-08-13T13:56:38Z,2024-16345,0,0,09000064866050dc
FDA-2022-N-0150-0010,FDA,FDA-2022-N-0150,"Revocation of Two Authorizations of Emergency Use of In Vitro Diagnostic
Device for Detection and/or Diagnosis of COVID–19; Availability",Notice,Announcement,2024-05-17T04:00:00Z,2024,5,2024-05-17T04:00:00Z,,2024-05-17T16:53:42Z,2024-10910,0,0,090000648656bb1f
FDA-2022-N-0150-0009,FDA,FDA-2022-N-0150,"Revocation of Two Authorizations of Emergency Use of In Vitro Diagnostic
Device for Detection and/or Diagnosis of COVID–19; Availability",Notice,Announcement,2024-02-06T05:00:00Z,2024,2,2024-02-06T05:00:00Z,,2024-02-06T15:43:24Z,2024-02356,0,0,09000064863e7e22