# K234070 (us_fda)

FDA 510(k) K234070 for Stelo Glucose Biosensor System (Mar 2024). OTC continuous glucose monitor.

## Key facts

- Jurisdiction: us_fda
- Filing type: fda_510k
- Status: cleared
- Filing number: K234070
- Filing date: 2024-03-05
- Decision date: 2024-03-05
- Verification posture: verified

## Applicant

- [Dexcom](/companies/dexcom.md)

## Covered models (1)

- [Stelo](/models/stelo.md)

## Sources (1)

- [https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K234070](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K234070)

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