Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K926060 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SYNCHRON CX7 Clinical System Part #: 756602 Product Usage: The Beckman SYNCHRON CX4 DELTA, CX7 D... | 2 | 10/27/2011 | Beckman Coulter Inc. |
SYNCHRON CX5 CE Clinical System Part #: 448700 Product Usage: The Beckman SYNCHRON CX4 DELTA, CX... | 2 | 10/27/2011 | Beckman Coulter Inc. |
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