Cordis Neurovascular, Inc. - FDA 510(k) Cleared Devices
37
Total
37
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Neurovascular, Inc. Cardiovascular ✕
25 devices
Cleared
Mar 14, 2007
MODIFICATION TO HYPERTRANSIT INFUSION CATHETER
Cardiovascular
44d
Cleared
Apr 18, 2005
HYPERTRANSIT INFUSION CATHETER
Cardiovascular
117d
Cleared
May 22, 2002
PROWLER SELECT (10, 14, AND PLUS) INFUSION CATHETERS WITH AND WITHOUT...
Cardiovascular
7d
Cleared
Mar 27, 2002
PROWLER SELECT 10 AND 14 INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS
Cardiovascular
23d
Cleared
Mar 01, 2001
MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES
Cardiovascular
8d
Cleared
Jan 08, 2001
PROWLER INFUSION CATHETERS WITH PRE-SHAPED TIPS
Cardiovascular
19d
Cleared
Apr 14, 2000
AGILITY STEERABLE GUIDEWIRE
Cardiovascular
14d
Cleared
Oct 28, 1999
PROWLER PLUS INFUSION CATHETER
Cardiovascular
28d
Cleared
Sep 23, 1999
AGILITY STEERABLE GUIDEWIRE
Cardiovascular
133d
Cleared
Aug 10, 1999
CORDIS ENDOVASCULAR TEMPORARY OCCLUSION BALLOON CATHETER
Cardiovascular
259d
Cleared
Sep 17, 1998
1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS
Cardiovascular
20d
Cleared
Feb 10, 1998
CES MASSTRANSIT INFUSION CATHETER
Cardiovascular
90d