510(k) K232033 · GEI Electrosurgical, Cutting & Coagulation & Accessories
HYBRIDknife® flex
| Applicant | Erbe Elektromedizin GmbH, Tuebingen, DE |
| Decision | Substantially Equivalent, Nov 29, 2023 |
| Received | Jul 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232033
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.