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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K071226
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Spectranetics Turbo-Booster Laser Guide Catheter, 8 Fr, REF 518-063, Sterile EO, Spectranetics Corpo... 2 08/04/2011 FEI # 3007284006
Spectranetics Corporation
Spectranetics Turbo-Booster Laser Guide Catheter, 7 Fr, REF 518-043, Sterile EO, Spectranetics Corpo... 2 08/04/2011 FEI # 3007284006
Spectranetics Corporation
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