ClearanceBrief
510(k) K760266 ยท DPS Electrocardiograph

MONITOR, ELECTROCARDIOSCOPE

ApplicantBurdick Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 13, 1976
ReceivedJul 22, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760266

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.