Regulations.gov document
Reference 5 - "Final Guidance for Industry & FDA: Updated 510(k) Sterility Review Guidance…
Supporting & Related Material · FDA-2009-D-0132 · posted Nov 8, 2010
Key facts
| Document ID | FDA-2009-D-0132-0018 |
|---|---|
| Title | Reference 5 - "Final Guidance for Industry & FDA: Updated 510(k) Sterility Review Guidance K90-1 (August 2002)" - [Guidance for Industry; Availability: Cellular Therapy for Cardiac Disease] |
| Document type | Supporting & Related Material |
| Subtype | REF-Reference (internal unless indicated) |
| Agency | FDA |
| Docket | FDA-2009-D-0132 |
| Posted | Nov 8, 2010 |
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: