ClearanceBrief
510(k) K801846 ยท DRX Electrode, Electrocardiograph

ELECTROCARDIOGRAPH ELECTRODE

ApplicantPhoenix Glove Co., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 9, 1980
ReceivedAug 4, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801846

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.