510(k) K253915 · GEI Electrosurgical, Cutting & Coagulation & Accessories
MOVIVA® Hybrid Ablation Probe
| Applicant | Erbe Elektromedizin GmbH, Tuebingen, DE |
| Decision | Substantially Equivalent, Dec 18, 2025 |
| Received | Dec 8, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253915
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.