ClearanceBrief
510(k) K901950 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

DITER ULTRASONIC S 3000

ApplicantDiter Elektroniikka OY, New York NY, US
DecisionSubstantially Equivalent, Jul 27, 1990
ReceivedMay 1, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901950

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.