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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K082129
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Binding Site Human IgM Kit (for SPAPLUS), REF: NK012.S The device consists of reaction buffer, sh... 2 11/17/2018 FEI # 3002808340
The Binding Site Group, Ltd.
Binding Site Human IgM Kit (for SPAPLUS), REF: NK012.S The device consists of reaction buffer, sh... 2 12/13/2018 FEI # 3002808340
The Binding Site Group, Ltd.
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