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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K033393
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Product Description
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Recall
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Guidant ABSOLUTE .035 Biliary Self-Expanding Stent System, 135 cm Length (Catheter), Base Part # FG... 2 06/07/2006 Guidant Endovascular Solutions, Inc.
Guidant ABSOLUTE .035 Biliary Self-Expanding Stent System, 135 cm Length (Catheter), Base Part #FG1... 2 06/07/2006 Guidant Endovascular Solutions, Inc.
ABSOLUTE .035 Biliary Self-Expanding Stent System, 135 cm Length (Catheter), Base Part #FG1010568.... 2 06/07/2006 Guidant Endovascular Solutions, Inc.
ABSOLUTE .035 Biliary Self-Expanding Stent System, 135 cm Length (Catheter)- Base Part #FG1010567.... 2 06/07/2006 Guidant Endovascular Solutions, Inc.
Guidant ABSOLUTE .035 Biliary Self-Expanding Stent System, 135 cm Length (Catheter), Base Part #FG... 2 06/07/2006 Guidant Endovascular Solutions, Inc.
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