Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K012210 |
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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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ACCU-CHEK Inform meter; catalog No. 3035123. | 2 | 12/28/2004 | Roche Diagnostics Corp. |
ACCU-CHEK Inform meter; catalog No. 3035123. | 2 | 07/20/2004 | Roche Diagnostics Corp. |
ACCU-CHEK Inform base unit; catalog no. 3035131. | 2 | 07/20/2004 | Roche Diagnostics Corp. |
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