K241138
- 510(k) number
- K241138
- Device name
- ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal Generator
- Applicant
- Livsmed, Inc. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-11-15
- Date received
- 2024-04-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241138.pdf
Official FDA record: K241138
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.