K-number	K150826
Device name	Nutra Face Lift Model PE8050
Applicant	Nutra Luxe MD, LLC
Product code	NFO
Device class	Class II
Decision date	Feb 10, 2016
Decision	Substantially Equivalent
Regulation	882.5890

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Source

View the full FDA submission: accessdata.fda.gov

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Nutra Face Lift Model PE8050

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