ClearanceBrief
510(k) K952978 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

ALTRA FLUX 110 HEMODIALYZER

ApplicantAlthin Medical AB an Affiliate of Baxter Intl, Miami Lakes FL, US
DecisionSubstantially Equivalent, Oct 5, 1995
ReceivedJun 27, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952978

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.