Medical Device Recalls
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1 result found
510(K) Number: K983047 |
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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 HQ for Blood Glucose Monitoring and Automated Data Management and Communication; Contents ... | 2 | 08/05/2006 | Roche Diagnostics Corp. |
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