Renal Solutions, Inc. is one of 5275 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renal Solutions, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Renal Solutions, Inc. has 9 FDA 510(k) cleared medical devices. Based in Apollo, US.
Historical record: 9 cleared submissions from 2003 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Renal Solutions, Inc. Filter by specialty or product code using the sidebar.
Renal Solutions, Inc. — FDA 510(k) Products and Clearance History
9 devices
Cleared
Feb 15, 2013
2008 HEMODIALYSIS SORBENT SYSTEM
Gastroenterology & Urology
64d
Cleared
Aug 17, 2012
VENOFER PUMP
Gastroenterology & Urology
88d
Cleared
Feb 10, 2011
VENOFER PUMP
Gastroenterology & Urology
66d
Cleared
Aug 13, 2010
2008 HEMODIALYSIS SORBENT SYSTEM
Gastroenterology & Urology
289d
Cleared
Jul 09, 2010
VENOFER PUMP
Gastroenterology & Urology
197d
Cleared
May 25, 2007
ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL# 1500
Gastroenterology & Urology
70d
Cleared
May 24, 2006
ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100
Gastroenterology & Urology
99d
Cleared
Jun 03, 2005
ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
Gastroenterology & Urology
158d
Cleared
Sep 17, 2003
SORB+HISORB+CARTRIDGE
Gastroenterology & Urology
163d