ClearanceBrief
510(k) K041942 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

M2376A DEVICELINK SYSTEM

ApplicantPhillips Medical Systems, Boblingen, DE
DecisionSubstantially Equivalent, Jul 23, 2004
ReceivedJul 19, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K041942

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.