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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K955797
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IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in serum and plasma Catalog Num... 2 12/03/2022 FEI # 1000361607
Randox Laboratories Ltd.
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