Medical Device Recalls
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1 result found
510(K) Number: K031002 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Opiate 300 Ng Reagent (OP 1 X 250) for use in conjunction with UniCel DxC 600/800 System(s) and SYNC... | 2 | 04/20/2020 |
FEI # 2050012 Beckman Coulter Inc. |
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