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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K160070
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Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A.... 2 03/13/2020 FEI # 3002808340
The Binding Site Group, Ltd.
Rheumatoid Factor (RF) Kit for use on SPAPLUS, Product #LK151.S.A Intended for the quantitative i... 2 02/08/2018 FEI # 3002808340
The Binding Site Group, Ltd.
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