ClearanceBrief
510(k) K870878 ยท DXK Echocardiograph

EUB-305 DIAGNOSTIC ULTRASOUND DEVICE

ApplicantHitachi Medical Corp. of America, Tarrytown NY, US
DecisionSubstantially Equivalent, Apr 22, 1988
ReceivedMar 4, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870878

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.