ClearanceBrief
510(k) K002784 ยท ITX Transducer, Ultrasonic, Diagnostic

ALOKA UST-5280-5

ApplicantAloka Co., Ltd., Wallingford CT, US
DecisionSubstantially Equivalent, Sep 20, 2000
ReceivedSep 6, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002784

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.