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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: K974306
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Quidel MicroVue Intact PTH EIA, Model 8044. An enzyme immunoassay for the quantification of Intact ... 3 04/25/2018 FEI # 1000122536
Diagnostic Hybrids, Inc.
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