K-number	K083278
Device name	AVC A/H5N1 FLU TEST
Applicant	Arbor Vita Corportation
Product code	OMS
Device class	Class II
Decision date	Apr 8, 2009
Decision	Substantially Equivalent
Regulation	866.3332

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View the full FDA submission: accessdata.fda.gov

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AVC A/H5N1 FLU TEST

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