510(k) K191542 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Apyx Plasma/RF Handpiece
| Applicant | Bovie Medical Corporation Dba Apyx Medical Corporation, Clearwater FL, US |
| Decision | Substantially Equivalent, Oct 11, 2019 |
| Received | Jun 11, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191542
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.