Regulations.gov document
Revocation of Two Authorizations of Emergency Use of In Vitro Diagnostic Devices for…
Notice · FDA-2022-N-0150 · posted Mar 9, 2023
Key facts
| Document ID | FDA-2022-N-0150-0008 |
|---|---|
| Title | Revocation of Two Authorizations of Emergency Use of In Vitro Diagnostic Devices for Detection and/or Diagnosis of COVID–19; Availability |
| Document type | Notice |
| Subtype | General Notice |
| Agency | FDA |
| Docket | FDA-2022-N-0150 |
| Posted | Mar 9, 2023 |
| Federal Register citation | 88 FR 14622 |
| FR document number | 2023-04845 |
| Comment period opens | Mar 9, 2023 |
| Effective date | Mar 9, 2023 |
At a glance
- 1–9 Pages
- None Public comments on this docket
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