AngioDynamics, Inc. - FDA 510(k) Cleared Devices
87
Total
82
Cleared
0
Denied
FDA 510(k) cleared devices by AngioDynamics, Inc. Gastroenterology & Urology ✕
10 devices
Cleared
Dec 06, 2024
NanoKnife Generator (H78720300301US0)
Gastroenterology & Urology
91d
Cleared
Mar 30, 2017
AngioDynamics Total Abscession Biliary Drainage Catheter
Gastroenterology & Urology
20d
Cleared
Jun 10, 2011
DURAFLOW 2 CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT
Gastroenterology & Urology
67d
Cleared
Oct 20, 2010
DURAMAX CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT
Gastroenterology & Urology
111d
Cleared
May 13, 2008
ANGIODYNAMICS, INC., DURAMAX HEMODIALYSIS CATHETER AND PROCEDURE KIT
Gastroenterology & Urology
90d
Cleared
Mar 09, 2006
ANGIODYNAMICS TOTAL ABSCESSION BILIARY DRAINAGE CATHETER
Gastroenterology & Urology
64d
Cleared
Apr 19, 2004
ANGIODYNAMICS, INC. MORE-FLOW HEMODIALYSIS CATHETER AND PROCEDURE KIT
Gastroenterology & Urology
62d
Cleared
Jul 31, 2000
ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER
Gastroenterology & Urology
49d
Cleared
Jun 25, 1999
ANGIODYNAMICS BALLOON EXPANDABLE BILIARY STENT SYSTEM
Gastroenterology & Urology
30d
Cleared
Jan 29, 1999
ANGIODYNAMICS ANGIOSTENT BILIARY STENT SYSTEM
Gastroenterology & Urology
207d