K261396
- 510(k) number
- K261396
- Device name
- Electric Wheelchair
- Applicant
- Ningbo Resshidi Medical Devices Co., Ltd. CN
- Product code
- ITI — Wheelchair, Powered
- Decision date
- 2026-07-08
- Date received
- 2026-04-29
- 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: K261396
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.