ClearanceBrief
510(k) K892006 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

HEALTHDYNE'S APNEA/HEART MONITOR, MODEL 900S

ApplicantHealthdyne, Inc., Marietta GA, US
DecisionSubstantially Equivalent, May 23, 1989
ReceivedMar 28, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K892006

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.