ClearanceBrief
510(k) K874421 ยท DRX Electrode, Electrocardiograph

PRE-GELLED DISPOSABLE ECG ELECTRODE - HP13941A

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Jan 28, 1988
ReceivedOct 28, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874421

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.