ClearanceBrief
510(k) K023569 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS

ApplicantSiemens Medical Solutions USA, Inc., Danvers MA, US
DecisionSubstantially Equivalent, Nov 4, 2002
ReceivedOct 24, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K023569

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.