ClearanceBrief
510(k) K952474 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

EAGLE 3000 PATIENT MONITOR

ApplicantMarquette Electronics, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Oct 19, 1995
ReceivedMay 30, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952474

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.