ClearanceBrief
510(k) K800536 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

MODEL H 607-.67M2 30 MICRON RP AN69 MEM

ApplicantHospal Medical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 7, 1980
ReceivedMar 10, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800536

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.