Cleared Traditional

K090885 - NEPHROS, INC., DSU DUAL STAGE ULTRAFILTER

K090885 is an FDA 510(k) clearance for NEPHROS, manufactured by Nephros, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FIP cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K090885 · Nephros, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2009
Decision
90d
Days
Class 2
Risk

K090885 is an FDA 510(k) clearance for the NEPHROS, INC., DSU DUAL STAGE ULTRAFILTER. Classified as Subsystem, Water Purification (product code FIP), Class II - Special Controls.

Submitted by Nephros, Inc. (River Edge, US). The FDA issued a Cleared decision on June 29, 2009 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5665 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Nephros, Inc. devices

FDA 510(k) Submission Details - K090885

510(k) Number K090885 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 2009
Decision Date June 29, 2009
Days to Decision 90 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 131d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FIP Device Classification - Class 2, Special Controls

Product Code FIP Subsystem, Water Purification
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5665
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FIP Subsystem, Water Purification

All 82
Devices cleared under the same product code (FIP) and FDA review panel - the closest regulatory comparables to K090885.
GAMBRO WATER PURIFICATION UNIT, MODELS WRO 300 AND WRO 300 H
K093608 · Gambro Renal Products, Inc. · Jul 2010
HEMODIALYSIS CARBON EXCHANGE, DUAL BED DEIONIZER EXCHANGE, MIXED BED DEIONIZER EXCHANGE, MODEL .60MAW,1.2MAW,3.6MAW, 1.2
K092481 · New Aqua, LLC (Dba Aqua Systems) · Apr 2010
WATER PURIFICATION COMPONENTS FOR HEMODIALYSIS
K083712 · Dipure, LLC · Jul 2009
DEIONIZER AND CARBON EXCHANGE SERVICE FOR HEMODIALYSIS
K082400 · Culligan Soft Water Service Co. · Feb 2009
BTI FILTRATION DEIONIZATION EXCHANGE TANK
K080703 · 4m Ventures, Inc. · Jun 2008
AQUA PURE DEIONIZER EXCHANGE SERVICE
K072158 · Staubach Barror Water Systems, Inc. · Feb 2008