K-number	K113063
Device name	CT-GUIDE NEEDLE GUIDANCE SYSTEM
Applicant	Activiews, Ltd.
Product code	JAK
Device class	Class II
Decision date	Nov 10, 2011
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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CT-GUIDE NEEDLE GUIDANCE SYSTEM

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