ClearanceBrief
510(k) K950471 ยท DRX Electrode, Electrocardiograph

DISPOSABLE ECG MONITORING ELECTRODE #4580 32X45MM

ApplicantNikomed U.S.A., Inc., Doylestown PA, US
DecisionSubstantially Equivalent, Nov 6, 1995
ReceivedFeb 3, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950471

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.