ClearanceBrief
510(k) K950688 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

OMIN-TRAK MODEL 3500 SERIES PATIENT MONITORING SYSTEM

ApplicantSafety Tek Corp., Orlando FL, US
DecisionSubstantially Equivalent, Apr 18, 1996
ReceivedFeb 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950688

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.