K-number	K233410
Device name	LIAISON PLEX Respiratory Flex Assay
Applicant	Luminex Corporation
Product code	QOF
Device class	Class II
Decision date	Mar 1, 2024
Decision	Substantially Equivalent
Regulation	866.3981

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Source

View the full FDA submission: accessdata.fda.gov

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LIAISON PLEX Respiratory Flex Assay

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