Medical Device Recalls
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1 result found
510(K) Number: K905845 |
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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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| LifePort, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816. | 2 | 11/17/2010 | Angiodynamics, INC |
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