ClearanceBrief
510(k) K023503 ยท DRX Electrode, Electrocardiograph

SKINTACT ECG ELECTRODE

ApplicantLeonhard Lang GmbH, Stillwater MN, US
DecisionSubstantially Equivalent, Nov 14, 2002
ReceivedOct 18, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K023503

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.