Leo Medical Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-12-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K241888 | Single-use Balloon Dilatation Catheter | FGE | 2024-12-20 | View |
| 510(k) | K172985 | Ligation Device | FHN | 2018-06-14 | View |
No matching devices.