Regulations.gov document
User Fees and Refunds for Premarket Notification Submissions (510(k)s): Guidance for…
Other · FDA-2003-D-0198 · posted Oct 2, 2017
Key facts
| Document ID | FDA-2003-D-0198-0003 |
|---|---|
| Title | User Fees and Refunds for Premarket Notification Submissions (510(k)s) : Guidance for Industry and Food and Drug Administration Staff |
| Document type | Other |
| Subtype | Guidance |
| Agency | FDA |
| Docket | FDA-2003-D-0198 |
| Posted | Oct 2, 2017 |
| Comment period opens | Oct 2, 2017 |
At a glance
- None 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: