Cordis, A Johnson & Johnson Co.
Cordis, A Johnson & Johnson Co. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2014.
Top product codes for Cordis, A Johnson & Johnson Co.
Recent clearances by Cordis, A Johnson & Johnson Co.
- K140286 — OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER
- K013581 — CORDIS AVIATOR PERIPHERAL DILATATION CATHETER
- K012090 — CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT
- K992755 — CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.