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510(k) K182456

Study Watch by Verily Life Sciences, LLC — Product Code DXH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 17, 2019
Date Received
September 7, 2018
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Transmitters And Receivers, Electrocardiograph, Telephone
Device Class
Class II
Regulation Number
870.2920
Review Panel
CV
Submission Type

Other clearances by Verily Life Sciences, LLC

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  • K192415 — Study Watch with Irregular Pulse Monitor (January 17, 2020)

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