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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K132750
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Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay in vitro diagnostic system for use on th... 3 12/23/2014 FEI # 3003218906
Illumina Inc
Illumina MiSeqDx Universal Kit 1.0, PN 15039608 The Illumina MiSeqDx Universal Kit 1.0 is a set o... 2 12/23/2014 FEI # 3003218906
Illumina Inc
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