ClearanceBrief
510(k) K060058 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

STELLAR 404T

ApplicantLarsen & Toubro Limited, Schaumburg IL, US
DecisionSubstantially Equivalent, Jan 20, 2006
ReceivedJan 9, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060058

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.