Medical Device Recalls
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1 result found
510(K) Number: K140496 |
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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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Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; an... | 2 | 04/17/2020 | Beckman Coulter Inc. |
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