Medical Device Recalls
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1 result found
510(K) Number: K873363 |
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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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Uric Acid plus ver.2 In vitro test for the quantitative determination of uric acid in human serum... | 2 | 06/27/2015 | Roche Diagnostics Operations, Inc. |
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