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FDA 510(k) Applications Submitted by CHRISTIE HUGHES
FDA 510(k) Number
Submission Date
Device Name
Applicant
K161495
06/01/2016
ARIES MI System, ARIES HSV 1&2 Assay Cassettes-Carton of 24 (IVD), ARIES HSV 1&2 Assay Protocol File Kit (IVD)
LUMINEX CORPORATION
K162772
10/03/2016
ARIES GBS Assay
LUMINEX CORPORATION
K133302
10/25/2013
FLEXMAP 3D
LUMINEX CORP.
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