ClearanceBrief
510(k) K832429 ยท DRX Electrode, Electrocardiograph

CARDIO TRACE ELECTRODE

ApplicantPoly-Med Splint Co., Mchenry IL, US
DecisionSubstantially Equivalent, May 9, 1984
ReceivedJul 22, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832429

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.