Medical Device Recalls
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1 result found
510(K) Number: K121790 |
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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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UniCel 600/800 Access Immunoassay Systems are in vitro diagnostic devices used for the quantitative,... | 2 | 09/23/2014 | Beckman Coulter Inc. |
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