FDA 510(k) Applications Submitted by KRISTINE SCHRAUFNAGEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090239 | 02/02/2009 | PROGASTRO CD ASSAY | PRODESSE, INC. |
| K092500 | 08/14/2009 | MODIFICATION TO PROFLU+ ASSAY | PRODESSE, INC. |
| K163281 | 11/21/2016 | FastStroke | GEf Medical Systems SCS |
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