K241090
- 510(k) number
- K241090
- Device name
- Evie Med Ring
- Applicant
- Movano Inc. Dba Movano Health CA · US
- Product code
- DQA — Oximeter
- Decision date
- 2024-11-29
- Date received
- 2024-04-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K241090.pdf
Official FDA record: K241090
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.