ClearanceBrief
510(k) K962293 ยท ITX Transducer, Ultrasonic, Diagnostic

ENDOSONICS AUTOMATIC PULL BACK DEVICE

ApplicantEndosonics Corp., Rancho Cordova CA, US
DecisionSubstantially Equivalent, Sep 16, 1996
ReceivedJun 14, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962293

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.