Regulations.gov document
510(k) Third Party Review Program and Third Party Emergency Use Authorization (EUA)…
Notice · FDA-2016-D-2565 · posted Dec 21, 2023
Key facts
| Document ID | FDA-2016-D-2565-0029 |
|---|---|
| Title | 510(k) Third Party Review Program and Third Party Emergency Use Authorization (EUA) Review; Draft Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations; Availability |
| Document type | Notice |
| Subtype | Notice of Availability |
| Agency | FDA |
| Docket | FDA-2016-D-2565 |
| Posted | Dec 21, 2023 |
| Federal Register citation | 88 FR 88395 |
| FR document number | 2023-28095 |
| Effective date | Dec 21, 2023 |
At a glance
- 1–9 Pages
- 10–99 Public comments on this docket
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Regulations.gov documents
Regulations.gov holds the rulemaking and other documents federal agencies post for public comment. Only agency documents are published here; public submissions are not.
Source: Regulations.gov (U.S. General Services Administration eRulemaking Program) · Source date: