K-number	K213971
Device name	Atrial Fibrillation History Feature
Applicant	Apple, Inc.
Product code	QDB
Device class	Class II
Decision date	Jun 3, 2022
Decision	Substantially Equivalent
Regulation	870.2790

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Source

View the full FDA submission: accessdata.fda.gov

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Atrial Fibrillation History Feature

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