Shenzhen Viatom Technology Co., Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories2
Latest FDA decision2025-02-28
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K242876 | Pulse Oximeter ( PO2, PO2A, PO2B) | DQA | 2025-02-28 | View |
| 510(k) | K203812 | Oxyfit Pulse Oximeter | DQA | 2022-11-08 | View |
| 510(k) | K193348 | Blood Pressure Monitor | DXN | 2020-06-25 | View |
| 510(k) | K191088 | Checkme O2 Pulse Oximeter | DQA | 2019-12-02 | View |
| 510(k) | K190207 | Blood Pressure Monitor | DXN | 2019-08-19 | View |
No matching devices.