ClearanceBrief
510(k) K103686 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

STAR 50 N

ApplicantLarsen & Toubro Limited, Crofton MD, US
DecisionSubstantially Equivalent, Mar 15, 2011
ReceivedDec 17, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103686

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.