K-number	K240627
Device name	LIAISON PLEX Yeast Blood Culture Assay
Applicant	Luminex Corporation
Product code	PEO
Device class	Class II
Decision date	Jun 4, 2024
Decision	Substantially Equivalent
Regulation	866.3365

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Source

View the full FDA submission: accessdata.fda.gov

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LIAISON PLEX Yeast Blood Culture Assay

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