Gi View , Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2023-08-17
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K230588 | Aer-O-Scope Colonoscope System | FDF | 2023-08-17 | View |
| 510(k) | K161791 | Aer-O-Scope Colonoscope System | FDF | 2016-08-11 | View |
No matching devices.