K-number	K163273
Device name	TRU Legionella
Applicant	Meridian Bioscience, Inc.
Product code	MJH
Device class	Class II
Decision date	Feb 21, 2017
Decision	Substantially Equivalent
Regulation	866.3300

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Source

View the full FDA submission: accessdata.fda.gov

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TRU Legionella

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