Medical Device Recalls
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1 result found
510(K) Number: K993706 |
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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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B-CrossLaps/serum (B-CTx in serum) REF 11972308 160 100 tests Immunoassay for the in vitro qua... | 2 | 07/12/2013 | Roche Diagnostics Operations, Inc. |
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