K-number	K163647
Device name	Revolve Envi 600 Advanced Adipose System
Applicant	Lifecell Corporation
Product code	MUU
Device class	Class II
Decision date	Aug 25, 2017
Decision	Substantially Equivalent
Regulation	878.5040

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Source

View the full FDA submission: accessdata.fda.gov

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Revolve Envi 600 Advanced Adipose System

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