Medical Device Recalls
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1 result found
510(K) Number: K980798 |
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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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| Detector H. Pylori, Catalog Number IHP-30 | 2 | 01/10/2024 |
FEI # 2244821 Immunostics, Inc. |
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