Cordis Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cordis Corporation - FDA 510(k) Cleared Devices
Recent clearances: ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire, SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands, SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
13
Total
12
Cleared
0
Denied
Cordis Corporation has 12 FDA 510(k) cleared cardiovascular devices. Based in Warren, US.
Last cleared in 2022. Active since 2004.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cordis Corporation
13 devices
Cleared
Apr 06, 2022
ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire
Cardiovascular
30d
Cleared
Feb 17, 2022
SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands
Cardiovascular
153d
Cleared
Apr 23, 2021
SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
Cardiovascular
52d
Cleared
Feb 26, 2021
Brite Tip Radianz Guiding Sheath
Cardiovascular
207d
Cleared
Oct 09, 2020
SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter
Cardiovascular
136d
Cleared
Sep 11, 2020
SABER .035 PTA Dilatation Catheter
Cardiovascular
115d
Cleared
Aug 15, 2018
RAIN Sheath Transradial
Cardiovascular
58d
Cleared
Apr 18, 2018
RAILWAY Sheathless Access System
Cardiovascular
97d
Cleared
Jan 14, 2015
ADROIT Guiding Catheter
Cardiovascular
47d
Cleared
Jun 27, 2014
SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER
Cardiovascular
191d
Cleared
Jun 14, 2012
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
Cardiovascular
30d
Cleared
Aug 03, 2004
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Gastroenterology & Urology
32d