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Luminex Gains FDA Clearance and CE-IVD Mark

July 6, 2016

Luminex has earned FDA clearance and CE-IVD mark approval for its ARIES M1 system, an in vitro diagnostic system, the company announced Wednesday.

The system is intended for lower throughput clinical labs and can process six different samples, and up to six assays at a time, the company said.

The system will be presented at the American Association of Clinical Chemistry’s Annual Scientific Meeting & Clinical Lab Expo in Philadelphia. — Anisa Jibrell

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