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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K964859
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Boston Scientific Impulse Flextrusion Shaft, Angiographic Catheter, Sterilized with ethylene oxide g... 2 09/04/2009 FEI # 3002095335
Boston Scientific Corporation
Boston Scientific Impulse Flextrusion Shaft 5F FR4 16391-02 H74916391022, (5-Pack Carton Label), Ang... 3 08/09/2007 FEI # 3001451463
Boston Scientific Corporation
Boston Scientific, Impulse Angiographic Catheter, Sterile EO. Catheters are single lumen catheters ... 2 01/31/2008 FEI # 3002095335
Boston Scientific
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