K-number	K240378
Device name	FAQ 201, FAQ 202
Applicant	Foreo, Inc.
Product code	OHS
Device class	Class II
Decision date	Apr 19, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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FAQ 201, FAQ 202

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FAQ 201, FAQ 202