Medical Device Recalls
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1 result found
510(K) Number: K203137 |
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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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| Venue Fit Models: R3 (Model Number H45303VFSC, H45303VFSW), R4 (Model Number H45314VFS, H45314VFSW),... | 2 | 04/11/2025 | GE Medical Systems, LLC |
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