ClearanceBrief
510(k) K781464 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

HEMODIALYZER, MODEL RP610, RP AN 69

ApplicantHospal Medical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 20, 1978
ReceivedAug 25, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781464

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.