Medical Device Recalls
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1 result found
510(K) Number: K974741 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Angiotech Breast Localization Needles: A) Accura BLN and Accura II BLN with Stiffening Cannula, ... | 2 | 07/13/2010 | Medical Device Technologies, Inc. |
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