ClearanceBrief
510(k) K936051 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

OMNI-CENTRAL STATION MONITOR

ApplicantInvivo Research, Inc., Orlando FL, US
DecisionSubstantially Equivalent, Jul 6, 1994
ReceivedDec 20, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K936051

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.