# K221774 (us_fda)

510(k) clearance for the Garmin ECG app (single-lead electrocardiogram); cleared 2023.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K221774
- Filing date: 2022-06-21
- Decision date: 2023-01-12
- Verification posture: verified

## Applicant

- [Garmin](/companies/garmin.md)

## Covered models (1)

- [Garmin (Venu / Fenix / Forerunner)](/models/garmin-watch.md)

## Sources (1)

- [https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221774](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221774)

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