Regulations.gov document
Draft Guidance for Industry and FDA Staff - Submission and review of sterility information…
Other · FDA-2008-D-0611 · posted Dec 12, 2008
Key facts
| Document ID | FDA-2008-D-0611-0002 |
|---|---|
| Title | Draft Guidance for Industry and FDA Staff - Submission and review of sterility information in premarket notification (510(k)) submissions for devices labeled as sterile - Guidance |
| Document type | Other |
| Subtype | GDL-Guidance (Supporting and Related Materials) |
| Agency | FDA |
| Docket | FDA-2008-D-0611 |
| Posted | Dec 12, 2008 |
At a glance
- 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: