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FDA 510(k) Applications Submitted by RONALD DUNN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K131565
05/30/2013
XTAG CYP2C19 KIT V3
LUMINEX MOLECULAR DIAGNOSTICS, INC.
K151906
07/13/2015
ARIES HSV 1&2 Assay Cassettes - Carton of 24 (IVD), ARIES HSV 1&2 Assay Protocol File Kit (IVD), ARIES HSV 1&2 Assay Cassette (IVD)
LUMINEX CORPORATION
K151917
07/13/2015
ARIES System
LUMINEX CORPORATION
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