ClearanceBrief
510(k) K861776 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

HIGH EFFICIENCY HEMODIALYSIS SYSTEM

ApplicantTravenol Laboratories, S.A., Deerfield IL, US
DecisionSubstantially Equivalent, Jun 19, 1986
ReceivedMay 8, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861776

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.