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Cordis, A Johnson & Johnson Co.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K013581 CORDIS AVIATOR PERIPHERAL DILATATION CATHETERDQY2001-11-28 View
510(k) K012090 CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENTFGE2001-08-01 View
510(k) K992755 CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBEFGE1999-09-15 View
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