Regulations.gov document
Revocation of Authorization of Emergency Use of In Vitro Diagnostic Device for Detection…
Notice · FDA-2022-N-0150 · posted Jul 25, 2024
Key facts
| Document ID | FDA-2022-N-0150-0011 |
|---|---|
| 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 | Announcement |
| Agency | FDA |
| Docket | FDA-2022-N-0150 |
| Posted | Jul 25, 2024 |
| Federal Register citation | 89 FR 60435 |
| FR document number | 2024-16345 |
| Comment period opens | Jul 25, 2024 |
| Effective date | Jul 25, 2024 |
At a glance
- 1–9 Pages
- None Public comments on this docket
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