Medical Device Recalls
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1 result found
510(K) Number: K951189 |
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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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| Synchron CX4, CX5 and CX9 Pro Systems. | 2 | 10/24/2003 | Beckman Coulter Inc |
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