ClearanceBrief
510(k) K880901 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

SONICATOR 710 (MODEL ME710)

ApplicantMettler Electronics Corp., Anaheim CA, US
DecisionSubstantially Equivalent, Mar 17, 1988
ReceivedMar 2, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880901

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.