K-number	K221698
Device name	Eargo 5 , Eargo 6
Applicant	Eargo, Inc.
Product code	QUH
Device class	Class II
Decision date	Dec 21, 2022
Decision	Substantially Equivalent
Regulation	874.3325

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Source

View the full FDA submission: accessdata.fda.gov

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Eargo 5 , Eargo 6

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