Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K003846 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ACCU-CHEK Inform meter; catalog No. 3035123. | 2 | 07/20/2004 |
FEI # 1823260 Roche Diagnostics Corp. |
| ACCU-CHEK Inform base unit; catalog no. 3035131. | 2 | 07/20/2004 |
FEI # 1823260 Roche Diagnostics Corp. |
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