Shenzhen Browiner Tech Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2024-12-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240841 | Digital Radiography System (ManntiX B, ManntiX K) | IZL | 2024-12-09 | View |
| 510(k) | K240284 | Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H) | IZL | 2024-03-28 | View |
No matching devices.