ClearanceBrief
510(k) K832659 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

BIOSPAL 1200S

ApplicantHospal Medical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 20, 1983
ReceivedAug 8, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832659

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.