ClearanceBrief
510(k) K140926 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

INMODE WMFACE DEVICE

ApplicantInmode MD , Ltd., Kfar Saba, IL
DecisionSubstantially Equivalent, Dec 3, 2014
ReceivedApr 11, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140926

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.