FDA 510(k) Applications Submitted by PRODESSE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K081030 | 04/11/2008 | MODIFICATION TO PROFLU+ ASSAY | PRODESSE, INC. |
| K091053 | 04/13/2009 | PROPARAFLU+ASSAY | PRODESSE, INC. |
| K082688 | 09/15/2008 | PRO HMPV+ ASSAY | PRODESSE, INC. |
| K073029 | 10/29/2007 | PROFLU+ ASSAY | PRODESSE, INC. |
| K090239 | 02/02/2009 | PROGASTRO CD ASSAY | PRODESSE, INC. |
| K092500 | 08/14/2009 | MODIFICATION TO PROFLU+ ASSAY | PRODESSE, INC. |
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