Medical Device Recalls
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1 result found
510(K) Number: K021827 |
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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 ACCU-Chek Active Meter Kit, Roche Diagnostics, Indianapolis, IN; REF 03184501001 includes the ... | 2 | 08/11/2009 | Roche Diagnostics Corp. |
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