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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