S40 CREATINE KINASE (CK) — Alfa Wassermann Diagnostic Technologies, Inc. (510(k) K082226)
S40 CREATINE KINASE (CK) — Alfa Wassermann Diagnostic Technologies, Inc. (510(k) K082226) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: S40 CREATINE KINASE (CK); Applicant: Alfa Wassermann Diagnostic Technologies, Inc.; Clearance track: 510(k).
| Device name | S40 CREATINE KINASE (CK) |
|---|---|
| Applicant | Alfa Wassermann Diagnostic Technologies, Inc. |
| Clearance track | 510(k) |
| Submission number | K082226 |
| Decision | Substantially Equivalent |
| Decision date | 2008-09-18 |
| Date received | 2008-08-07 |
| Product code | JHS |
| Device class | 2 |
| Medical specialty | Clinical Chemistry |
| Applicant location | NJ, US |
| Source | openFDA device |
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