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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 36 Results
510(K) Number: K033134
 
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery system 5... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 7... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 7... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 7... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 6... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 6... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 6... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 6... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 5... 2 07/20/2004 FEI # 2183870
ev3, Inc.
ParaMount Mini GPS Stent System, Peripheral System, Balloon Expandable Stent and Delivery System 5... 2 07/20/2004 FEI # 2183870
ev3, Inc.
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