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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K160517
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Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in c... 2 08/19/2019 Luminex Corporation
ARIES Extraction Kit; ARIES System; SYNCT , REF 50-10026, UDI # 00840487100073 2 08/15/2019 Luminex Corporation
ARIES System and ARIES M1 System 2 05/16/2017 Luminex Corporation
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