Medical Device Recalls
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1 result found
510(K) Number: K150052 |
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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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TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative m... | 2 | 06/01/2020 | Trividia Health, Inc. |
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