K253918
- 510(k) number
- K253918
- Device name
- Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)
- Applicant
- F Care Systems USA, LLC FL · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-06-02
- Date received
- 2025-12-08
- 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: K253918.pdf
Official FDA record: K253918
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.