K-number	K201680
Device name	NuFACE Mini Plus
Applicant	Carole Cole Company
Product code	NFO
Device class	Class II
Decision date	Feb 19, 2021
Decision	Substantially Equivalent
Regulation	882.5890

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Source

View the full FDA submission: accessdata.fda.gov

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NuFACE Mini Plus

Everything you need for a 510(k) submission. Nothing you don't.