Applied Medical
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2021-12-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K202818 | Voyant Fine Fusion Device (EB230) | GEI | 2021-12-16 | View |
| 510(k) | K191866 | GelPOINT Mini Advanced Access Platform | GCJ | 2020-04-29 | View |
No matching devices.