Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K952875 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ACCU-CHEK Instant Meter; Catalog numbers 914 and 924. | 2 | 07/13/2005 |
FEI # 1823260 Roche Diagnostics Corp. |
| ACCU-CHEK Instant Care Kit; Catalog number 91490. | 2 | 07/13/2005 |
FEI # 1823260 Roche Diagnostics Corp. |
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