Genexel-Sein, Inc.
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) | K080853 | DUO-CARE BLOOD GLUCOSE AND BLOOD PRESSURE MONITOR SYSTEM | NBW | 2009-02-20 | View |
| 510(k) | K071523 | FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODELS BP1600, BP1650, BP1700 AND BP1750 | DXN | 2007-06-26 | View |
No matching devices.
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