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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K980453
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FDA Recall
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Boston Scientific 6F Guider Softip XF Guiding Catheter, 6 French, 40 degree angle, 90cm usable lengt... 3 11/24/2007 FEI # 2939204
Boston Scientific Target
Boston Scientific 6F Guider Softip XF Guiding Catheter, 6 French, 40 degree angle, 100cm usable len... 3 11/24/2007 FEI # 2939204
Boston Scientific Target
Guider XF Softip Guide Catheter, manufactured by Boston Scientific Corporation, Maple Grove, MN, dis... 2 11/20/2009 FEI # 2939204
Boston Scientific Corporation
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