ClearanceBrief
510(k) K080173 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

STAR 55

ApplicantLarsen & Toubro Limited, Schaumburg IL, US
DecisionSubstantially Equivalent, Feb 8, 2008
ReceivedJan 24, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080173

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.