ClearanceBrief
510(k) K983689 ยท DRX Electrode, Electrocardiograph

BLUE SENSOR SUPATAB,DISPOSABLE ECG ELECTRODES

ApplicantMedicotest A/S, Washington DC, US
DecisionSubstantially Equivalent, Jan 15, 1999
ReceivedOct 20, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983689

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.