K-number	K131804
Device name	REMEL XPECT FLU A&B
Applicant	Remel, Inc.
Product code	GNX
Device class	Class I
Decision date	Jul 12, 2013
Decision	Substantially Equivalent
Regulation	866.3330

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View the full FDA submission: accessdata.fda.gov

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REMEL XPECT FLU A&B

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