Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K161495 |
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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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ARIES HSV 1&2 Assay, Catalog/REF# 50-10017 | 2 | 02/02/2022 | Luminex Corporation |
ARIES HSV 1&2 Assay, Part Number/REF 50-10017 | 2 | 01/14/2022 | Luminex Corporation |
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 HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295 | 2 | 08/15/2019 | Luminex Corporation |
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