Medical Device Recalls
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1 result found
510(K) Number: K033734 |
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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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Roche Diagnostics LightCycler Capillaries (100uL) for use in conjunction with the LightCycler analyz... | 2 | 12/12/2007 | Roche Diagnostics Corp. |
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