Medical Device Recalls
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1 result found
510(K) Number: K032557 |
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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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Vortex TR, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816 | 2 | 11/17/2010 | Angiodynamics, INC |
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