ClearanceBrief
510(k) K910665 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

MODEL 556 MONITOR W/24-HR. TREND RECALL/MODIFIED

ApplicantGe Medical Systems Information Technologies, Wallingford CT, US
DecisionSubstantially Equivalent, Dec 31, 1991
ReceivedFeb 11, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910665

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.