K250068
- 510(k) number
- K250068
- Device name
- Venclose digiRF Generator (VCRFG1)
- Applicant
- Venclose, Inc. CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-02-04
- Date received
- 2025-01-10
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K250068.pdf
Official FDA record: K250068
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.