510(k) K213971

Atrial Fibrillation History Feature by Apple, Inc. — Product Code QDB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 2022
Date Received
December 20, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Photoplethysmograph Analysis Software For Over-The-Counter Use
Device Class
Class II
Regulation Number
870.2790
Review Panel
CV
Submission Type

A photoplethysmograph analysis software device for over-the-counter use analyzes photoplethysmograph data and provides information for identifying irregular heart rhythms. This device is not intended to provide a diagnosis.