Medical Device Recalls
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1 result found
510(K) Number: K940295 |
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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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| Uroview 2600 Uroview System | 2 | 06/21/2003 |
FEI # 1720753 GE OEC Medical Systems,Inc |
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