ClearanceBrief
510(k) K903839 ยท DXK Echocardiograph

INTERSPEC APOGEE

ApplicantInterspec, Inc., Ambler PA, US
DecisionSubstantially Equivalent, Nov 16, 1990
ReceivedAug 21, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903839

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.