Regulations.gov document
The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications…
Other · FDA-2011-D-0652 · posted Jul 28, 2014
Key facts
| Document ID | FDA-2011-D-0652-0033 |
|---|---|
| Title | The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications [510(k)]; Guidance for Industry and Food and Drug Administra tion Staff |
| Document type | Other |
| Subtype | Guidance |
| Agency | FDA |
| Docket | FDA-2011-D-0652 |
| Posted | Jul 28, 2014 |
| Comment period opens | Jul 28, 2014 |
At a glance
- 10–99 Public comments on this docket
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