Medical Device Recalls
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1 result found
510(K) Number: K984402 |
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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 Ammonia (AMM) Reagent Product Usage: AMM reagent, when used in conjunction with SYNCHRO... | 2 | 04/16/2012 | Beckman Coulter Inc. |
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