ClearanceBrief
510(k) K821368 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

MODELS 78504A & 78508A PATIENT MON. SYS

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, May 25, 1982
ReceivedMay 10, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821368

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.