ClearanceBrief
510(k) K862618 ยท DRX Electrode, Electrocardiograph

SKINTACT AG ELECTRODES

ApplicantLeon H. Lang Co., Archenweg, 56, AT
DecisionSubstantially Equivalent, Sep 15, 1986
ReceivedJul 9, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862618

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.