Regulations.gov document
30-Day Notices, 135-Day Premarket Approval Supplements and 75-Day Humanitarian Device…
Other · FDA-1998-D-0281 · posted Apr 13, 2011
Key facts
| Document ID | FDA-1998-D-0281-0002 |
|---|---|
| Title | 30-Day Notices, 135-Day Premarket Approval Supplements and 75-Day Humanitarian Device Exemption Supplements for Manufacturing Method or Process Changes; Guidance for Industry and FDA Staff |
| Document type | Other |
| Subtype | GDL-Guidance (Supporting and Related Materials) |
| Agency | FDA |
| Docket | FDA-1998-D-0281 |
| Posted | Apr 13, 2011 |
| Comment period opens | Apr 13, 2011 |
At a glance
- 1–9 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: