Medical Device Recalls
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1 result found
510(K) Number: K060620 |
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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 Aviva Meter Kit, Roche Diagnostics, Indianapolis, IN; REF 04893247001 includes the R... | 2 | 08/11/2009 | Roche Diagnostics Corp. |
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