ClearanceBrief
510(k) K862544 ยท DPS Electrocardiograph

KENZ-ECG-102 SINGLE CHANNEL ELECTROCARDIOGRAPH

ApplicantSuzuken Co., Ltd., Indianapolis IN, US
DecisionSubstantially Equivalent, Aug 6, 1986
ReceivedJul 3, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862544

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.