ClearanceBrief
510(k) K832877 ยท DRX Electrode, Electrocardiograph

PRE-GELLED DISPOS ELECTRODE

ApplicantAdvance Tech Intl., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 22, 1983
ReceivedAug 26, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832877

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.