Medical Device Recalls
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1 result found
510(K) Number: K983617 |
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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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| DiaSorin 25-HydroxyvitaminD [125I] RIA Kit. For the quantitative determination of 25-OH-D and other... | 3 | 04/13/2005 |
FEI # 2182595 Diasorin Inc. |
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