Cordis, A Johnson & Johnson Co. - FDA 510(k) Cleared Devices
Recent clearances: OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER, CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE
4
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis, A Johnson & Johnson Co. Cardiovascular ✕
2 devices