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withdrawn,object_id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-0150-0018,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,2026-01-02T05:00:00Z,2026,1,2026-01-02T05:00:00Z,,2026-01-02T20:34:16Z,2025-24155,0,0,09000064b9114f6c
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
FDA-2022-N-0150-0016,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,2025-06-26T04:00:00Z,2025,6,2025-06-26T04:00:00Z,,2025-06-26T17:45:21Z,2025-11822,0,0,09000064b8e3225c
FDA-2022-N-0150-0015,FDA,FDA-2022-N-0150,Revocation of Four Authorizations of Emergency Use of In Vitro Diagnostic Devices for Detection and/or Diagnosis of COVID–19; Availability,Notice,Announcement,2025-05-29T00:00:00Z,2025,5,2025-05-29T00:00:00Z,,2025-05-29T17:31:38Z,2025-09678,0,0,09000064b8dc7841
FDA-2022-N-0150-0014,FDA,FDA-2022-N-0150,Revocation of Three Authorizations of Emergency Use of In Vitro Diagnostic Devices for Detection and/or Diagnosis of COVID–19; Availability,Notice,Announcement,2025-03-20T04:00:00Z,2025,3,,,2025-03-20T18:40:40Z,2025-04710,0,0,0900006486a12c61
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
FDA-2022-N-0150-0008,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,2023-03-09T05:00:00Z,2023,3,2023-03-09T05:00:00Z,,2023-03-09T15:45:11Z,2023-04845,0,0,0900006485781d64
FDA-2022-N-0150-0007,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,2022-11-04T04:00:00Z,2022,11,2022-11-04T04:00:00Z,,2022-11-04T14:25:30Z,2022-24072,0,0,09000064854883e3
FDA-2022-N-0150-0006,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,2022-09-09T04:00:00Z,2022,9,2022-09-09T04:00:00Z,,2022-09-09T16:36:13Z,2022-19491,0,0,09000064852d875d
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
FDA-2022-N-0150-0004,FDA,FDA-2022-N-0150,Revocation of Authorization of Emergency Use of an In Vitro Diagnostic Device for Detection and/or Diagnosis of COVID–19; Availability,Notice,Announcement,2022-05-24T04:00:00Z,2022,5,2022-05-24T04:00:00Z,,2022-05-24T15:12:34Z,2022-11122,0,0,09000064850dbdb0
FDA-2022-N-0150-0003,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,2022-05-09T04:00:00Z,2022,5,2022-05-09T04:00:00Z,,2022-05-12T16:57:33Z,2022-09887,0,0,09000064850612f9
FDA-2022-N-0150-0002,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,2022-03-14T04:00:00Z,2022,3,2022-03-14T04:00:00Z,,2022-03-14T13:11:29Z,2022-05310,0,0,0900006484fc6980
FDA-2022-N-0150-0001,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,2022-03-04T05:00:00Z,2022,3,2022-03-04T05:00:00Z,,2022-03-04T15:49:04Z,2022-04635,0,0,0900006484fb9ebc