ClearanceBrief
510(k) K831944 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

PATIENT MONITOR #78832A

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 19, 1983
ReceivedJun 16, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831944

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.