Technidyne Corp.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K930068 | HEMOCHRON MODEL 8000/FACTOR VI PREMIER COAGULATION | JPA | 1993-09-02 | View |
| 510(k) | K930235 | HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY | GGP | 1993-09-02 | View |
No matching devices.
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