ClearanceBrief
510(k) K240070 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Profound Matrix

ApplicantCandela Corporation, Marlborough MA, US
DecisionSubstantially Equivalent, Jul 1, 2024
ReceivedJan 9, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240070

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.