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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