ClearanceBrief
510(k) K861359 ยท DPS Electrocardiograph

CARDIAC MONITOR, CARDIOTACHOMETER AND ALARM

ApplicantHewlett-Packard Co., Waltham MA, US
DecisionSubstantially Equivalent, May 16, 1986
ReceivedApr 10, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861359

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.