Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K070585 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Roche ACCU-CHEK Performa blood glucose meters/kits, Roche Diagnostics, Indianapolis, IN. Test s... | 2 | 09/16/2009 |
FEI # 1823260 Roche Diagnostics Corp. |
| Roche ACCU-CHEK Performa blood glucose test strips, Roche Diagnostics, Indianapolis, IN. Test s... | 2 | 09/16/2009 |
FEI # 1823260 Roche Diagnostics Corp. |
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