ClearanceBrief
510(k) K903710 ยท DXK Echocardiograph

WASHINGTON CARDIAC MONITOR

ApplicantWashington Biolab, Inc., Ames IA, US
DecisionSubstantially Equivalent, Nov 9, 1990
ReceivedAug 14, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903710

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.