K-number	K212372
Device name	Fitbit Irregular Rhythm Notifications
Applicant	Fitbit, Inc.
Product code	QDB
Device class	Class II
Decision date	Apr 8, 2022
Decision	Substantially Equivalent
Regulation	870.2790

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Source

View the full FDA submission: accessdata.fda.gov

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Fitbit Irregular Rhythm Notifications

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