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FDA 510(k) Applications Submitted by Wendy Ricker
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160517
02/24/2016
ARIES System
LUMINEX CORPORATION
K161220
04/29/2016
ARIES« Flu A/B & RSV Assay
LUMINEX CORPORATION
K171441
05/16/2017
ARIES C. difficile Assay Complete Kit, ARIES C. difficile Assay Protocol File Kit, ARIES C. difficile Assay Kit (24 cassettes), ARIES Stool Resuspension Kit
Luminex Corporation
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