ClearanceBrief
510(k) K831787 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

PATIENT MONITOR #78353A

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 29, 1983
ReceivedJun 3, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831787

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.