ClearanceBrief
510(k) K790939 ยท DPS Electrocardiograph

MODEL 78501A PATIENT MONITORING SYSTEM

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 11, 1979
ReceivedMay 18, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790939

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.