ClearanceBrief
510(k) K231790 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

The InMode System with the Morpheus8 Applicators

ApplicantInMode , Ltd., Yokneam Illit, IL
DecisionSubstantially Equivalent, Jul 20, 2023
ReceivedJun 20, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K231790

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.