Shenzhenshi Sincoheren S&T Development Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-10-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231749 | Radio Frequency System | GEI | 2023-10-19 | View |
| 510(k) | K231894 | LED Spectrum therapy instrument | GEX | 2023-09-20 | View |
No matching devices.