ClearanceBrief
510(k) K901032 ยท DPS Electrocardiograph

PCI MODEL 2041-PC TELEMETRY MONITOR W/ARRHYTHMIA

ApplicantAccucore, Inc., Santa Ana CA, US
DecisionSubstantially Equivalent, Apr 4, 1990
ReceivedMar 6, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901032

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.