Medical Device Recalls
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1 result found
510(K) Number: K103037 |
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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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HealthyWiser UriTest" UTI Test Strips REF 900-UTI | 2 | 10/23/2023 | Universal Meditech Inc. |
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