K253707
- 510(k) number
- K253707
- Device name
- Electric wheelchair (W1,W3)
- Applicant
- Shenzhen Zhimahuaerkai Technology Co., Ltd. CN
- Product code
- ITI — Wheelchair, Powered
- Decision date
- 2026-02-24
- Date received
- 2025-11-24
- 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: K253707
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.