K232505
- 510(k) number
- K232505
- Device name
- Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter
- Applicant
- Zhejiang Curaway Medical Technology Co., Ltd. CN
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-05-30
- Date received
- 2023-08-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232505.pdf
Official FDA record: K232505
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.