Chf Solutions, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Chf Solutions, Inc. has 13 FDA 510(k) cleared gastroenterology & urology devices. Based in Washington, US.
Historical record: 13 cleared submissions from 2002 to 2020.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Chf Solutions, Inc.
13 devices
Cleared
Feb 24, 2020
Aquadex FlexFlow System 2.0
Gastroenterology & Urology
147d
Cleared
Sep 07, 2007
AQUADEX FLEXFLOW SYSTEM
Gastroenterology & Urology
64d
Cleared
Apr 27, 2007
MODIFICATION TO AQUADEX FLEXFLOW SYSTEM
Gastroenterology & Urology
64d
Cleared
Dec 13, 2006
MODIFICATION TO AQUADEX FLEXFLOW SYSTEM
Gastroenterology & Urology
76d
Cleared
Feb 02, 2006
AQUADEX FLEXFLOW SYSTEM
Gastroenterology & Urology
30d
Cleared
Nov 09, 2005
AQUADEX SYSTEM
Gastroenterology & Urology
244d
Cleared
Sep 10, 2004
5.2F DUAL LUMEN EXTENDED LENGTH CATHETER (DELC)
Gastroenterology & Urology
70d
Cleared
Apr 27, 2004
AQUADEX SYSTEM 100, MODEL A1100
Gastroenterology & Urology
61d
Cleared
Dec 23, 2003
DUAL LUMEN EXTENDED LENGTH CATHETER (DELC)
Gastroenterology & Urology
204d
Cleared
Nov 20, 2003
SYSTEM 100 ULTRAFILTRATION CATHETER
Gastroenterology & Urology
364d
Cleared
Mar 14, 2003
SYSTEM 100-UF 500 CIRCUIT WITH IN-LINE NEEDLELESS ACCESS PORT
Gastroenterology & Urology
88d
Cleared
Oct 25, 2002
INFUSION CATHETER EXTENSION SET
Gastroenterology & Urology
28d