ClearanceBrief
510(k) K770023 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

MONITOR, NEONATE, MODEL 78213A

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 28, 1977
ReceivedJan 6, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770023

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.