ClearanceBrief
510(k) K061816 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

GALAXY

ApplicantLarsen & Toubro Limited, Schaumburg IL, US
DecisionSubstantially Equivalent, Jul 12, 2006
ReceivedJun 28, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061816

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.