FDA 510(k) Applications Submitted by CORDIS, A JOHNSON & JOHNSON CO.

FDA 510(k) Number Submission Date Device Name Applicant
K012090 07/05/2001 CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT CORDIS, A JOHNSON & JOHNSON CO.
K992755 08/16/1999 CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE CORDIS, A JOHNSON & JOHNSON CO.
K013581 10/29/2001 CORDIS AVIATOR PERIPHERAL DILATATION CATHETER CORDIS, A JOHNSON & JOHNSON CO.
K140286 02/05/2014 OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER CORDIS, A JOHNSON & JOHNSON CO.


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