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