K261075
- 510(k) number
- K261075
- Device name
- Manual Wheelchair (MS01);Manual Wheelchair (MA01)
- Applicant
- GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd. CN
- Product code
- IOR — Wheelchair, Mechanical
- Decision date
- 2026-06-22
- Date received
- 2026-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K261075.pdf
Official FDA record: K261075
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.