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18 rows where docket_id = "FDA-2022-N-0150" sorted by posted_date descending
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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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0150-0018 | 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;