FDA 510(k) Applications Submitted by DENNIS TASCHEK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082226 | 08/07/2008 | S40 CREATINE KINASE (CK) | ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
| K083040 | 10/14/2008 | S-TEST C-REACTIVE PROTEIN (CRP) | ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
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