Gi Supply, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-04-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221042 | Renova RP Centesis Pump | BTA | 2023-04-19 | View |
| 510(k) | K202376 | EverLift Submucosal Lifting Agent | PLL | 2020-09-30 | View |
No matching devices.