ClearanceBrief
510(k) K242688 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Finiff System

ApplicantSkingrab Co., Ltd., Seoul, KR
DecisionSubstantially Equivalent, Dec 20, 2024
ReceivedSep 6, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242688

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.