Medical Device Recalls
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1 result found
510(K) Number: K123256 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Human Alpha-1-Antitrypsin Kit for use on the SPAPlus analyser, Product #NK034.S. The firm name on t... | 2 | 10/04/2017 |
FEI # 3002808340 The Binding Site Group, Ltd. |
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