Cordis Neurovascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cordis Neurovascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TRUFILL DCS SYRINGE, TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE OR TRUFILL DCS SYRINGE II, ALSO KNOWN AS THE TRUFILL DCS ORBIT, VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER)
37
Total
37
Cleared
0
Denied
Cordis Neurovascular, Inc. has 37 FDA 510(k) cleared medical devices. Based in Miami Lakes, US.
Historical record: 37 cleared submissions from 1994 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cordis Neurovascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cordis Neurovascular, Inc.
37 devices
Cleared
Sep 12, 2008
TRUFILL DCS SYRINGE
Neurology
29d
Cleared
May 02, 2008
TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE OR TRUFILL DCS...
Neurology
28d
Cleared
Sep 26, 2007
VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER)
Neurology
72d
Cleared
Mar 14, 2007
MODIFICATION TO HYPERTRANSIT INFUSION CATHETER
Cardiovascular
44d
Cleared
Dec 07, 2006
THE TRUFILL DCS DETACHABLE COIL SYSTEM
Neurology
41d
Cleared
Dec 15, 2005
TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM LINE EXTENSION
Neurology
29d
Cleared
Apr 18, 2005
HYPERTRANSIT INFUSION CATHETER
Cardiovascular
117d
Cleared
Sep 23, 2003
TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS...
Neurology
35d
Cleared
Jun 20, 2003
TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS THE...
Neurology
85d
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
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