Endogi Medical, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2023-09-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232596 | EndoGI S-Path Biliary Stent System | FGE | 2023-09-27 | View |
| 510(k) | K193600 | EndoGI Biliary Stent System | FGE | 2020-06-26 | View |
No matching devices.