ClearanceBrief
510(k) K864868 ยท DRX Electrode, Electrocardiograph

MICROPOROUS MONITORING ELECTRODES & ADAPTER BLOCK

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Jan 14, 1987
ReceivedDec 12, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864868

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.