Medical Device Recalls
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1 result found
510(K) Number: K860478 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Sterling Diagnostics, Inc. Serum Iron/IBC (Colorimetric) for IN VITRO DIAGNOSTIC USE in the quantita... | 3 | 12/29/2016 | Sterling Diagnostics, Inc. |
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