ClearanceBrief
510(k) K874562 ยท DRX Electrode, Electrocardiograph

SECURATRODE

ApplicantMeddev International Corp., Los Altos CA, US
DecisionSubstantially Equivalent, Jan 28, 1988
ReceivedNov 4, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874562

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.