K241723
- 510(k) number
- K241723
- Device name
- Electric wheelchair (W3902)
- Applicant
- Zhejiang Richall Medical Technology Co., Ltd. CN
- Product code
- ITI — Wheelchair, Powered
- Decision date
- 2024-09-05
- Date received
- 2024-06-14
- 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: K241723
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.