K-number	K110406
Device name	CELLTRACKS AUTOPREP SYSTEM
Applicant	Veridex, LLC
Product code	NQI
Device class	Class II
Decision date	Jan 20, 2012
Decision	Substantially Equivalent
Regulation	866.6020

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Source

View the full FDA submission: accessdata.fda.gov

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CELLTRACKS AUTOPREP SYSTEM

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