Diagnostica Stago
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) | K162227 | STA® - Liatest® D-Di | DAP | 2016-12-10 | View |
| 510(k) | K010455 | ROTACHROM HEPARIN AND STA -ROTACHROM HEPARIN | KFF | 2001-06-07 | View |
No matching devices.
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