ClearanceBrief
510(k) K040121 ยท IMG Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat

DERMAWAVE 5000 COMBI MAX SYSTEM

ApplicantDermawave, LLC, Loxahatchee FL, US
DecisionSubstantially Equivalent, Mar 17, 2004
ReceivedJan 20, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040121

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.