K141731 is an FDA 510(k) clearance for the NEPHROS DSU-H, NEPHROS SSU-H. This device is classified as a System, Water Purification, General Medical Use (Class II - Special Controls, product code NHV).
Submitted by Nephros, Inc. (River Edge, US). The FDA issued a Cleared decision on October 24, 2014, 119 days after receiving the submission on June 27, 2014.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5665. The Device Is A Portable Water Treatment System Which Features Components And Technology Similar To Water Treatment Systems Previously Cleared For Hemodialysis. The Difference Lies With The Intended Use, As The Proposed Device Is Not Intended For Use In Hemodialysis Applications, For Which A Product Code Currently Exists. Instead, The Proposed Device Is Intended For Use To Purify Water For General Purposes, Including Washing Of Surgeons Hands, Surgical Instruments, And Wound Cleansing..