Medical Device Recalls
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1 result found
510(K) Number: K050943 |
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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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| ViewPoint; system, imaging processing, radiological | 2 | 09/13/2024 |
FEI # 3004497354 GE Healthcare GmbH |
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