ClearanceBrief
510(k) K790507 ยท DRX Electrode, Electrocardiograph

800 ECG ELECTRODE

ApplicantSimonsen & Weels Eftf., Mchenry IL, US
DecisionSubstantially Equivalent, May 18, 1979
ReceivedMar 13, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790507

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.