ClearanceBrief
510(k) K760150 ยท DPS Electrocardiograph

MONITOR, PATIENT (MODEL 78331A)

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 19, 1976
ReceivedJul 1, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760150

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.