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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