K-number	K133605
Device name	BD MAX MRSA XT, BD MAX INSTRUMENT
Applicant	Geneohm Sciences Canada, Inc.
Product code	NQX
Device class	Class II
Decision date	Dec 20, 2013
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 XT, BD MAX INSTRUMENT

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