510(k) K213357 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone
Study Watch with Irregular Pulse Monitor (Home), Study Watch with Irregular Pulse Monitor
| Applicant | Verily Life Sciences, LLC, South San Francisco CA, US |
| Decision | Substantially Equivalent, Jul 19, 2022 |
| Received | Oct 12, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213357
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.