K250126
- 510(k) number
- K250126
- Device name
- ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M)
- Applicant
- Livsmed, Inc. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-10-21
- Date received
- 2025-01-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250126.pdf
Official FDA record: K250126
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.