ClearanceBrief
510(k) K900032 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

MODEL M1175A/M1176A WITH ST SEGMENT MONITORING

ApplicantHewlett-Packard Co., Waltham MA, US
DecisionSubstantially Equivalent, Apr 10, 1990
ReceivedJan 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900032

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.