Regulations.gov document
Revocation of Authorization of Emergency Use of In Vitro Diagnostic Device for Detection…
Notice · FDA-2022-N-0150 · posted Sep 3, 2024
Key facts
| Document ID | FDA-2022-N-0150-0012 |
|---|---|
| Title | Revocation of Authorization of Emergency Use of In Vitro Diagnostic Device for Detection and/or Diagnosis of COVID–19; Availability |
| Document type | Notice |
| Subtype | General Notice |
| Agency | FDA |
| Docket | FDA-2022-N-0150 |
| Posted | Sep 3, 2024 |
| Federal Register citation | 89 FR 71372 |
| FR document number | 2024-19724 |
| Effective date | Sep 3, 2024 |
At a glance
- 1–9 Pages
- None Public comments on this docket
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