K-number	K100684
Device name	CELLTRACKS AUTOPREP SYSTEM MODEL:9541
Applicant	Veridex, LLC
Product code	GKH
Device class	Class I
Decision date	Aug 26, 2010
Decision	Substantially Equivalent
Regulation	864.5240

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View the full FDA submission: accessdata.fda.gov

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CELLTRACKS AUTOPREP SYSTEM MODEL:9541

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