ClearanceBrief
510(k) K241138 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal Generator

ApplicantLivsmed, Inc., Seongnam-Si, KR
DecisionSubstantially Equivalent, Nov 15, 2024
ReceivedApr 24, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241138

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.