Irregular Rhythm Notification Feature— 510(k) DEN180042

Unknown

Apple, Inc.

FDA 510(k) clearance DEN180042 for Irregular Rhythm Notification Feature, Unknown on 2018-09-11. Applicant: Apple, Inc..

Clearance details

Applicant: Apple, Inc.
Product code: Code QDB
Advisory panel: Cardiovascular
Date received: 2018-08-09
Decision date: 2018-09-11
Decision: Unknown
Clearance type: Direct
Location: Alexandria, VA, US

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