ClearanceBrief
510(k) K061590 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

SMDIE DEVICE INTERFACING SYSTEM

ApplicantSiemens Medical Solutions Health Services Corporat, Clearwater FL, US
DecisionSubstantially Equivalent, Jun 21, 2006
ReceivedJun 8, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061590

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.