ClearanceBrief
510(k) K922974 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

PORTABLE PATIENT MONITOR

ApplicantHewlett-Packard Co., Waltham MS, US
DecisionSubstantially Equivalent, Dec 7, 1992
ReceivedJun 22, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922974

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.