ClearanceBrief
510(k) K781518 ยท DRX Electrode, Electrocardiograph

PREGELLED DISPOSABLE ELECTRODE

ApplicantVente Medical Products, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 6, 1978
ReceivedAug 31, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781518

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.