Heuron Co., Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories3
Latest FDA decision2024-05-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K233247 | Heuron ICH | QAS | 2024-05-15 | View |
| 510(k) | K231642 | Veuron-Brain-pAb3 | LLZ | 2023-10-13 | View |
| 510(k) | K203279 | Veuron-Brain-mN1 | LNH | 2022-07-12 | View |
| 510(k) | K213801 | Veuron-Brain-pAb2 | LLZ | 2022-02-04 | View |
| 510(k) | K203142 | Veuron-Brain-pAb | LLZ | 2021-01-15 | View |
No matching devices.