ClearanceBrief
510(k) K960802 ยท IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

CUSHMAN MANUFACTURING, INC. ULTRA 6.0.

ApplicantCushman Mfg., Inc., Long Beach CA, US
DecisionSubstantially Equivalent, Jun 18, 1996
ReceivedFeb 27, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960802

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.