Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K160070 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 | 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 | The Binding Site Group, Ltd. |
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