K-number	K083464
Device name	PREMIER CAMPY, MODEL 618096
Applicant	Meridian Bioscience, Inc.
Product code	LQP
Device class	Class I
Decision date	Jan 30, 2009
Decision	Substantially Equivalent
Regulation	866.3110

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Source

View the full FDA submission: accessdata.fda.gov

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PREMIER CAMPY, MODEL 618096

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