ClearanceBrief
510(k) K880602 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

MODIFIED SONICATOR 720, MODEL ME720

ApplicantMettler Electronics Corp., Anaheim CA, US
DecisionSubstantially Equivalent, Feb 25, 1988
ReceivedFeb 11, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880602

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.