510(k) K223262 · GEI Electrosurgical, Cutting & Coagulation & Accessories
Renuvion® APR Handpiece
| Applicant | Apyx Medical Corporation, Clearwater FL, US |
| Decision | Substantially Equivalent, Feb 23, 2023 |
| Received | Oct 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223262
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.