ClearanceBrief
510(k) K771360 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

ECG SCOPE MODEL 7833

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 4, 1977
ReceivedJul 25, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K771360

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.