Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K132750 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Illumina MiSeqDx Universal Kit 1.0, PN 15039608 The Illumina MiSeqDx Universal Kit 1.0 is a set o... | 2 | 12/23/2014 | Illumina Inc |
Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay in vitro diagnostic system for use on th... | 3 | 12/23/2014 | Illumina Inc |
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