510(k) K946279

PRISMA CFM (CONTINUOUS FLUID MANAGEMENT SYSTEM) by Cobe Renal Care, Inc. — Product Code KDI

K946279 is an FDA 510(k) premarket notification submitted by Cobe Renal Care, Inc. for the device "PRISMA CFM (CONTINUOUS FLUID MANAGEMENT SYSTEM)". The FDA issued a decision of Substantially Equivalent on February 10, 1997. 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. Cobe Renal Care, Inc. has at least 10 other 510(k) clearances on record.