ClearanceBrief
510(k) K790454 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

MODEL 78801A PATIENT MONITORS

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 3, 1979
ReceivedMar 5, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790454

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.