Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K093514 |
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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| Discovery 670 DR Model # H3100BT | 2 | 09/21/2020 |
FEI # 2126677 GE Healthcare, LLC |
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