Radisen Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2022-08-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213520 | AXIR-CX | LLZ | 2022-08-19 | View |
| 510(k) | K221144 | PEDRA-1417MC, PEDRA-1417MG, PEDRA-1417FC, PEDRA-1417FG | MQB | 2022-05-13 | View |
No matching devices.