ClearanceBrief
510(k) K170826 ยท KDN System, Perfusion, Kidney

Perfadex Plus

ApplicantXvivo Perfusion AB, Sloane, SE
DecisionSubstantially Equivalent, Jun 22, 2018
ReceivedMar 20, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170826

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.