Medical Device Recalls
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1 result found
510(K) Number: K860154 |
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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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Urea Nitrogen/Color BUN (Enzymatic Berthelot) for IN VITRO DIAGNOSTIC USE in the quantitative determ... | 3 | 12/29/2016 | Sterling Diagnostics, Inc. |
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