ClearanceBrief
510(k) K040784 ยท DRX Electrode, Electrocardiograph

PROTAB ECG TABB ELECTRODE

ApplicantBio Protech, Inc., Crofton MD, US
DecisionSubstantially Equivalent, Apr 7, 2004
ReceivedMar 29, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040784

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.