Cordis Corporation

13 FDA 510(k) medical device clearances.

Top product codes for Cordis Corporation

LIT — Cardiovascular 5 devices
DYB — Cardiovascular 3 devices
DQO — Cardiovascular 1 device
DQY — Cardiovascular 1 device
DTK — Cardiovascular 1 device
FGE — Gastroenterology, Urology 1 device
NTE — Cardiovascular 1 device

Recent clearances by Cordis Corporation

K220654 — ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire NTE · 2022-04-06
K212977 — SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands DQO · 2022-02-17
K210626 — SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter LIT · 2021-04-23
K202167 — Brite Tip Radianz Guiding Sheath DYB · 2021-02-26
K201377 — SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter LIT · 2020-10-09
K201333 — SABER .035 PTA Dilatation Catheter LIT · 2020-09-11
K181592 — RAIN Sheath Transradial DYB · 2018-08-15
K180081 — RAILWAY Sheathless Access System DYB · 2018-04-18
K143412 — ADROIT Guiding Catheter DQY · 2015-01-14
K133843 — SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER LIT · 2014-06-27
K121442 — POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER LIT · 2012-06-14
K041796 — PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM FGE · 2004-08-03
K034050 — CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F DTK · 2004-03-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.