K240990
- 510(k) number
- K240990
- Device name
- Mobility Scooter
- Applicant
- Zhejiang Innuovo Rehabilitation Devices Co.,Ltd CN
- Product code
- INI — Vehicle, Motorized 3-Wheeled
- Decision date
- 2024-09-10
- Date received
- 2024-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K240990
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.