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Cordis, A Johnson & Johnson Co.

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER (K140286)Cordis, A Johnson & Johnson Co.2014-03-07
CORDIS AVIATOR PERIPHERAL DILATATION CATHETER (K013581)Cordis, A Johnson & Johnson Co.2001-11-28
CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT (K012090)Cordis, A Johnson & Johnson Co.2001-08-01
CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE (K992755)Cordis, A Johnson & Johnson Co.1999-09-15

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Every clearance here is in the API, with alerts when new ones post.