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

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

18 rows where docket_id = "FDA-2022-N-0150" sorted by posted_date descending

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Suggested facets: title, subtype, posted_month, posted_date (date), comment_start_date (date), last_modified (date)

posted_year 5

  • 2022 7
  • 2024 5
  • 2025 4
  • 2023 1
  • 2026 1

document_type 1

  • Notice 18

agency_id 1

  • FDA 18
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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 None 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

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CREATE TABLE documents (
    id TEXT PRIMARY KEY,
    agency_id TEXT,
    docket_id TEXT REFERENCES dockets(id),
    title TEXT,
    document_type TEXT,
    subtype TEXT,
    posted_date TEXT,
    posted_year INTEGER,
    posted_month INTEGER,
    comment_start_date TEXT,
    comment_end_date TEXT,
    last_modified TEXT,
    fr_doc_num TEXT,
    open_for_comment INTEGER,
    withdrawn INTEGER,
    object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;
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