510(k) K261203

multiFiltratePRO System by Fresenius Medical Care Renal Therapies Group, LLC — Product Code KDI

K261203 is an FDA 510(k) premarket notification submitted by Fresenius Medical Care Renal Therapies Group, LLC for the device "multiFiltratePRO System". The FDA issued a decision of Substantially Equivalent on Oct 19, 2026. The device falls under product code KDI (Dialyzer, High Permeability With Or Without Sealed Dialysate System), a Class II device regulated under 21 CFR 876.5860. Fresenius Medical Care Renal Therapies Group, LLC has 52 other 510(k) clearances on record.