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FDA 510(k) Applications Submitted by Verily Life Sciences LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K192415
09/04/2019
Study Watch with Irregular Pulse Monitor
Verily Life Sciences LLC
K213357
10/12/2021
Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor
Verily Life Sciences LLC
K182456
09/07/2018
Study Watch
Verily Life Sciences LLC
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