ClearanceBrief
510(k) K000645 ยท DPS Electrocardiograph

GE MARQUETTE MEDICAL SYSTEMS PRUCKA CARDIOLAB CATH SYSTEM, VERSION 1.11

ApplicantGeneral Electric Medical Systems Information Techn, Sugarland TX, US
DecisionSubstantially Equivalent, May 24, 2000
ReceivedFeb 25, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000645

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.