This article was originally published Jan. 8.

SAN FRANCISCO — Illumina has submitted its MiSeqDx system and two cystic fibrosis assays to the US Food and Drug Administration for 510(k) clearance, company officials said this week during a presentation at the JP Morgan Healthcare conference in San Francisco.

The company said last November that it planned to submit the system and assay to the FDA (CSN 11/1/2012).

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