ClearanceBrief
510(k) K760271 ยท DPS Electrocardiograph

ELECTROCARDIOGRAPH, EK-7 (3-CHANNELS)

ApplicantBurdick Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 15, 1976
ReceivedJul 22, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760271

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.