# K212372 (us_fda)

FDA 510(k) K212372 for Fitbit Irregular Rhythm Notifications / AFib detection (Apr 2022).

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K212372
- Filing date: 2022-04-08
- Decision date: 2022-04-08
- Verification posture: verified

## Applicant

- [Fitbit](/companies/fitbit.md)

## Covered models (1)

- [Fitbit (Charge / Sense / Versa)](/models/fitbit-tracker.md)

## Sources (1)

- [https://www.accessdata.fda.gov/cdrh_docs/pdf21/K212372.pdf](https://www.accessdata.fda.gov/cdrh_docs/pdf21/K212372.pdf)

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