Nephros Receives 510(k) Clearance for Hemodiafiltration System

May 1, 2012
Nephros announced it has received 510(k) clearance from the FDA to market its Hemodiafiltration system for the treatment of  chronic renal failure when used with controlled dialysis machines capable of producing ultrapure dialysate in accordance with current AAMI/ANSI/ISO standards in the United States.
The Sacramento Bee