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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K862044
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DELFIA® hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code... 2 04/27/2019 FEI # 3002808498
PerkinElmer Life and Analytical Sciences, Wallac, OY
AutoDELFIA® hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product ... 2 04/27/2019 FEI # 3002808498
PerkinElmer Life and Analytical Sciences, Wallac, OY
AutoDELFIA® hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product ... 2 04/27/2019 FEI # 3002808498
PerkinElmer Life and Analytical Sciences, Wallac, OY
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