ClearanceBrief
510(k) K041907 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

TRIO MONITOR

ApplicantDatascope Corp., Mahwh NJ, US
DecisionSubstantially Equivalent, Jul 23, 2004
ReceivedJul 15, 2004
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K041907

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.