K-number	K222012
Device name	FAQ 101
Applicant	Foreo, Inc.
Product code	PAY
Device class	Class II
Decision date	Apr 5, 2023
Decision	Substantially Equivalent
Regulation	878.4420

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Source

View the full FDA submission: accessdata.fda.gov

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FAQ 101

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