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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: K001005
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Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used with Wako L-Type HDL-C or L-Type LD... 3 01/28/2021 FEI # 1000513161
Fujifilm Medical Systems U.S.A., Inc.
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