ClearanceBrief
510(k) K982134 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

DYNAMIC HOLLOW FIBER DIALYZER DS-SERIES MODEL AS-851

ApplicantDynamic Technology Corp., Hsinchu, TW
DecisionSubstantially Equivalent, Apr 14, 1999
ReceivedJun 17, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982134

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.