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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K143653
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Verigene Processor SP, Models 10-0000-07/10-0000-07R a component of the Verigene system 2 05/13/2022 FEI # 3002524000
Luminex Corporation
Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024 2 07/02/2021 FEI # 3006028115
Luminex Corporation
Verigene Processor SP, Model Numbers 10-0000-07 and 10-0000-07R. Used with assay: Luminex, VERIGENE... 2 11/20/2020 FEI # 3006028115
Luminex Corporation
Verigene Processor SP, Model Numbers 10-0000-07 and 10-0000-07R. Used with assay Luminex, VERIGENE ... 2 11/20/2020 FEI # 3006028115
Luminex Corporation
VERIGENE Processor SP Model No. 10-0000-07. An in vitro diagnostic device intended for processing ... 2 10/05/2020 FEI # 3002524000
Luminex Corporation
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