K-number	K120138
Device name	BD MAX MRSA ASSAY, BD MAX INSTRUMENT
Applicant	Bd Diagnostics (Geneohm Sciences Canada, Inc)
Product code	NQX
Device class	Class II
Decision date	Jul 5, 2012
Decision	Substantially Equivalent
Regulation	866.1640

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View the full FDA submission: accessdata.fda.gov

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BD MAX MRSA ASSAY, BD MAX INSTRUMENT

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