Medical Device Recalls
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1 result found
510(K) Number: K060768 |
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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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| FreeStyle Precision H Blood Glucose and Ketone Monitoring System, UDI: 00093815711810 | 2 | 02/28/2020 | Abbott Diabetes Care, Inc. |
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