Apyx Medical Corporation (Formerly Bovie Medical Corporation
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2022-05-25
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K211652 | Renuvion Dermal Handpiece, Renuvion Dermal System | GEI | 2022-05-25 | View |
| 510(k) | K202880 | J-Plasma Precise FLEX Handpiece | GEI | 2021-01-04 | View |
No matching devices.