ClearanceBrief
510(k) K821434 ยท DRX Electrode, Electrocardiograph

EKG (ECG) ELECTRODES

ApplicantDupaco, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 30, 1982
ReceivedMay 12, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821434

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.