K-number	K990640
Device name	VELOGENE RAPID MRSA IDENTIFICATION ASSAY
Applicant	Id Biomedical Corp.
Product code	MYI
Device class	Class II
Decision date	Jul 9, 1999
Decision	Substantially Equivalent
Regulation	866.1640

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View the full FDA submission: accessdata.fda.gov

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VELOGENE RAPID MRSA IDENTIFICATION ASSAY

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