510(k) K211652 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Renuvion Dermal Handpiece, Renuvion Dermal System
| Applicant | Apyx Medical Corporation (Formerly Bovie Medical Corporation, Clearwater FL, US |
| Decision | Substantially Equivalent, May 25, 2022 |
| Received | May 28, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211652
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.