Medical Device Recalls
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1 result found
510(K) Number: K884689 |
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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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Active Cortisol EIA, 96 Wells, DSL-10-2000 The DSL-10-2000 Active Cortisol Enzyme Immunoassay (EI... | 2 | 07/08/2011 | Beckman Coulter Inc. |
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