Aktiia SA
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2025-07-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250415 | G0 Blood Pressure Monitoring System (G0) | DXN | 2025-07-02 | View |
No matching devices.
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