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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: K040431
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Tina-quant IgM Gen.2, Catalog Nos. 03507190190, 05220726190, 03507041190, 03507149190 Product Usa... 2 04/13/2019 FEI # 1823260
Roche Diagnostics Corporation
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