Company ยท US
Prodesse, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2009. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 20, 2009 | K091053 | PROPARAFLU+ASSAY Prodesse, Inc. | OOU |
| Aug 20, 2009 | K092500 | MODIFICATION TO PROFLU+ ASSAY Prodesse, Inc. | OCC |
| Apr 16, 2009 | K090239 | PROGASTRO CD ASSAY Prodesse, Inc. | LLH |
| Nov 7, 2008 | K082688 | PRO HMPV+ ASSAY Prodesse, Inc. | OEM |
| May 2, 2008 | K081030 | MODIFICATION TO PROFLU+ ASSAY Prodesse, Inc. | OCC |
| Jan 4, 2008 | K073029 | PROFLU+ ASSAY Prodesse, Inc. | OCC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||