K-number	K113319
Device name	ROTOR-GENE Q MDX
Applicant	QIAGEN GmbH
Product code	OOI
Device class	Class II
Decision date	Feb 6, 2012
Decision	Substantially Equivalent
Regulation	862.2570

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Source

View the full FDA submission: accessdata.fda.gov

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ROTOR-GENE Q MDX

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