Medical Device Manufacturer · US , New York , NY

Nephros, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2005

8

Total

8

Cleared

0

Denied

Nephros, Inc. has 8 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 8 cleared submissions from 2005 to 2017. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Nephros, Inc. Filter by specialty or product code using the sidebar.

Nephros, Inc. is one of 4730 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nephros, Inc.

8 devices

1-8 of 8

Cleared Mar 02, 2017

Gastroenterology & Urology · 296d

Cleared Dec 22, 2016

HydraGuard 10 UltraFilter

Gastroenterology & Urology · 209d

Cleared Apr 08, 2016

Gastroenterology & Urology · 165d

Cleared Oct 24, 2014

NEPHROS DSU-H, NEPHROS SSU-H

Gastroenterology & Urology · 119d

Cleared Apr 27, 2012

NEPHROS OLPUR H2H HEMODIAFILTRATION (HDF) MODULE AND OLPUR MD 220 HEMODIAFILTER

Gastroenterology & Urology · 260d

Cleared Jul 14, 2011

NEPHROS DSU FILTER, NEPHROS MSU FILTER, NEPHROS SSU FILTER

Gastroenterology & Urology · 164d

Cleared Jun 29, 2009

NEPHROS, INC., DSU DUAL STAGE ULTRAFILTER

Gastroenterology & Urology · 90d

Cleared Jun 09, 2005

OLPUR DIALYZER, MODEL HD 190

Gastroenterology & Urology · 92d