ClearanceBrief
510(k) K030050 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

TORAYSULFONE DIALYZER, BS-L SERIES

ApplicantToray Industries (America), Inc., Bellaire TX, US
DecisionSubstantially Equivalent, Sep 29, 2003
ReceivedJan 6, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030050

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.