ClearanceBrief
510(k) K033283 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

CENTRA VIEW DEVICE LINK SYSTEM

ApplicantIcu Datasystems, Inc., Gainesville FL, US
DecisionSubstantially Equivalent, Oct 27, 2003
ReceivedOct 14, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033283

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.