510(k) K250688 · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cedar Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar Endovenous Radiofrequency Catheter (ERA-C30-US); Endovenous Radiofrequency Generator (ERA-G5-US)
| Applicant | Acotec Scientific Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Oct 7, 2025 |
| Received | Mar 6, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250688
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.