K-number	K093346
Device name	BD GENEOHM MRSA ACP ASSAY
Applicant	Bd Diagnostics (Geneohm Sciences, Inc.)
Product code	NQX
Device class	Class II
Decision date	Dec 15, 2009
Decision	Substantially Equivalent
Regulation	866.1640

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View the full FDA submission: accessdata.fda.gov

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BD GENEOHM MRSA ACP ASSAY

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