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Cordis Corporation

13 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire (K220654)Cordis Corporation2022-04-06
SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands (K212977)Cordis Corporation2022-02-17
SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter (K210626)Cordis Corporation2021-04-23
Brite Tip Radianz Guiding Sheath (K202167)Cordis Corporation2021-02-26
SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter (K201377)Cordis Corporation2020-10-09
SABER .035 PTA Dilatation Catheter (K201333)Cordis Corporation2020-09-11
RAIN Sheath Transradial (K181592)Cordis Corporation2018-08-15
RAILWAY Sheathless Access System (K180081)Cordis Corporation2018-04-18
ADROIT Guiding Catheter (K143412)Cordis Corporation2015-01-14
SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER (K133843)Cordis Corporation2014-06-27
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER (K121442)Cordis Corporation2012-06-14
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM (K041796)Cordis Corporation2004-08-03
CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F (K034050)Cordis Corporation2004-03-22

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Every clearance here is in the API, with alerts when new ones post.