Cordis Corporation - FDA 510(k) Cleared Devices
Recent clearances: ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire, SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands, SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
13
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Corporation Gastroenterology & Urology ✕
1 devices