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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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