Kabi Diagnostica
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) | K902393 | COACUTE ANTITHROMBIN CHROMOGENIC ASSAY | JBQ | 1990-09-25 | View |
| 510(k) | K901874 | COATEST LMW HEPARIN/HEPARIN CHROMOGENIC ASSAY | KFF | 1990-07-20 | View |
No matching devices.
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