Medical Device Recalls
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1 result found
510(K) Number: K881495 |
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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 CX5 Clinical System Part #: 759300 Product Usage: The Beckman SYNCHRON CX4 DELTA, CX7 D... | 2 | 10/27/2011 | Beckman Coulter Inc. |
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