Prodesse, Inc.
FDA Regulatory Profile
Prodesse, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on November 20, 2009.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K091053 | PROPARAFLU+ASSAY | November 20, 2009 |
| K092500 | MODIFICATION TO PROFLU+ ASSAY | August 20, 2009 |
| K090239 | PROGASTRO CD ASSAY | April 16, 2009 |
| K082688 | PRO HMPV+ ASSAY | November 7, 2008 |
| K081030 | MODIFICATION TO PROFLU+ ASSAY | May 2, 2008 |
| K073029 | PROFLU+ ASSAY | January 4, 2008 |