510(k) K220206
K220206 is an FDA 510(k) premarket notification submitted by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd for the device "Mobility Scooter". The FDA issued a decision of Substantially Equivalent on Mar 24, 2022. The device falls under product code INI (Vehicle, Motorized 3-Wheeled), a Class II device regulated under 21 CFR 890.3800. Zhejiang Innuovo Rehabilitation Devices Co.,Ltd has 19 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 24, 2022
- Date Received
- Jan 25, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Vehicle, Motorized 3-Wheeled
- Device Class
- Class II
- Regulation Number
- 890.3800
- Review Panel
- PM
- Submission Type
- 510(k)