ClearanceBrief
510(k) K081552 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

SKYLINE 55

ApplicantLarsen & Toubro Limited, Mysore, Karnataka, IN
DecisionSubstantially Equivalent, Jul 31, 2008
ReceivedJun 3, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081552

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.