510(k) K161134 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator
| Applicant | Bovie Medical Corporation, Clearwater FL, US |
| Decision | Substantially Equivalent, Jun 20, 2016 |
| Received | Apr 22, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161134
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.