K-number	K141173
Device name	AMPLIVUE GAS ASSAY
Applicant	Quidel Corporation
Product code	PGX
Device class	Class II
Decision date	Jul 24, 2014
Decision	Substantially Equivalent
Regulation	866.2680

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Source

View the full FDA submission: accessdata.fda.gov

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AMPLIVUE GAS ASSAY

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