Regulations.gov document
Draft Guidance for Industry and Food and Drug Administration Staff The 510(k) Program…
Other · FDA-2011-D-0652 · posted Dec 28, 2011
Key facts
| Document ID | FDA-2011-D-0652-0002 |
|---|---|
| Title | Draft Guidance for Industry and Food and Drug Administration Staff The 510(k) Program Evaluating Substantial Equivalence in Premarket Notifications [510(k)] |
| Document type | Other |
| Subtype | Guidance |
| Agency | FDA |
| Docket | FDA-2011-D-0652 |
| Posted | Dec 28, 2011 |
| Comment period opens | Dec 28, 2011 |
| Comments due | Apr 27, 2012 |
At a glance
- No Open for comment
- 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: