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FDA 510(k) Applications Submitted by Cordis Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K181592
06/18/2018
RAIN Sheath Transradial
Cordis Corporation
K143412
11/28/2014
ADROIT Guiding Catheter
CORDIS CORPORATION
K202167
08/03/2020
Brite Tip Radianz Guiding Sheath
Cordis Corporation
K121442
05/15/2012
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
CORDIS CORPORATION
K034050
12/30/2003
CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F
CORDIS CORPORATION
K220654
03/07/2022
ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire
Cordis Corporation
K041796
07/02/2004
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
CORDIS CORPORATION
K133843
12/18/2013
SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER
CORDIS CORPORATION
K201333
05/19/2020
SABER .035 PTA Dilatation Catheter
Cordis Corporation
K201377
05/26/2020
SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter
Cordis Corporation
K180081
01/11/2018
RAILWAY Sheathless Access System
Cordis Corporation
K212977
09/17/2021
SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands
Cordis Corporation
K210626
03/02/2021
SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
Cordis Corporation
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