ClearanceBrief
510(k) K223110 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

truSculpt iD

ApplicantCutera, Inc., Brisbane CA, US
DecisionSubstantially Equivalent, Nov 3, 2022
ReceivedOct 3, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K223110

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.