510(k) K243120 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
HybridAPC probe
| Applicant | Erbe Elektromedizin GmbH, Tuebingen, DE |
| Decision | Substantially Equivalent, Jun 20, 2025 |
| Received | Sep 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243120
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.