Cordis Corp. - FDA 510(k) Cleared Devices
Recent clearances: FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM, POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER, ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE
315
Total
281
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Corp. Microbiology ✕
5 devices