K254141
- 510(k) number
- K254141
- Device name
- Manual Wheelchair (DY01903(2))
- Applicant
- Guangdong Dayang Medical Technology Co., Ltd. CN
- Product code
- IOR — Wheelchair, Mechanical
- Decision date
- 2026-05-21
- Date received
- 2025-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K254141.pdf
Official FDA record: K254141
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.