ClearanceBrief
510(k) K181954 ยท CAC Apparatus, Autotransfusion

autoLog IQ Autotransfusion System

ApplicantMedtronic Perfusion Systems, Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 22, 2018
ReceivedJul 23, 2018
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K181954

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.