Ev3 Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ev3 Corporation - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Ev3 Corporation has 4 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 4 cleared submissions from 2003 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ev3 Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ev3 Corporation
5 devices
Cleared
Jun 17, 2005
PROTEGE RX GPS SELF-EXPANDING NITRINOL STENT
Gastroenterology & Urology
21d
Cleared
Apr 20, 2005
PROTEGE GPS SELF-EXPANDING NITINOL STENT
Gastroenterology & Urology
30d
Cleared
Sep 08, 2004
X-SIZER CATHETER SYSTEM
Cardiovascular
888d
Cleared
Jun 24, 2003
NITREX NITINOL GUIDEWIRE
Cardiovascular
8d
Cleared
Jan 24, 2003
NITREX NITINOL GUIDEWIRE
Cardiovascular
50d