K-number	K171069
Device name	ZELTIQ CoolSculpting System
Applicant	Zeltiq Aesthetics, Inc.
Product code	OOK
Device class	Class II
Decision date	Jul 7, 2017
Decision	Substantially Equivalent
Regulation	878.4340

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Source

View the full FDA submission: accessdata.fda.gov

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ZELTIQ CoolSculpting System

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