K232763
- 510(k) number
- K232763
- Device name
- Electrode Handpieces (VCT, RFTV, BMDT series)
- Applicant
- RF Medical Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2023-10-04
- Date received
- 2023-09-08
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232763.pdf
Official FDA record: K232763
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.