Medical Device Recalls
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1 result found
510(K) Number: K090920 |
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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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Human lgG4 Subclass Liquid Reagent Kits Human lgG1& lgG2 Antisera, lgG3 & 4 Latex reagent and lgG An... | 2 | 01/23/2017 | The Binding Site Group, Ltd. |
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