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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K042152
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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 FEI # 3002808340
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 FEI # 3002808340
The Binding Site Group, Ltd.
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