Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K042152 |
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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 kit for use on the Beckman Coulter AU" series This kit is intended for qualify... | 2 | 01/23/2017 | The Binding Site Group, Ltd. |
Human Subclass Kit for use on the Beckman IMMAGE"/IMMAGE"800 Analyser Product Code LK009.IM This ... | 2 | 01/23/2017 | The Binding Site Group, Ltd. |
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