Cordis Corporation
FDA 510(k) medical device clearances.
Top product codes for Cordis Corporation
Recent clearances by Cordis Corporation
- K220654 — ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire
- K212977 — SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands
- K210626 — SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
- K202167 — Brite Tip Radianz Guiding Sheath
- K201377 — SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter
- K201333 — SABER .035 PTA Dilatation Catheter
- K181592 — RAIN Sheath Transradial
- K180081 — RAILWAY Sheathless Access System
- K143412 — ADROIT Guiding Catheter
- K133843 — SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER
- K121442 — POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
- K041796 — PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
- K034050 — CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F
Data sourced from openFDA. This site is unofficial and independent of the FDA.