Medical Device Recalls
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1 result found
510(K) Number: K060323 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Boston Scientific Ultraflex Precision Colonic Stent System Material/UPN/Catalog Number: M00557360 | 2 | 08/31/2010 | Boston Scientific Corporation |
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