510(k) K232505 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter
| Applicant | Zhejiang Curaway Medical Technology Co., Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, May 30, 2024 |
| Received | Aug 18, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232505
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.