Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K160517 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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