ClearanceBrief
510(k) K871668 ยท DRX Electrode, Electrocardiograph

BIODAN TYPE COMET ELECTRODE

ApplicantNational Medical Technology, Quebec, Canada, CA
DecisionSubstantially Equivalent, Jun 10, 1987
ReceivedApr 28, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871668

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.