Medical Device Recalls
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1 result found
510(K) Number: K120568 |
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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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FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic Use only. Use only with... | 1 | 05/09/2013 | Abbott Diabetes Care, Inc. |
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