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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: K993853
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K-Assay(R) Multi-Analyte Calibrator, REF KAI--016C, KAMIYA BIOMEDICAL COMPANY, Seattle, WA, IVD The... 2 10/20/2017 FEI # 2084025
Kamiya Biomedical Company, LLC
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