K261149
- 510(k) number
- K261149
- Device name
- Electric Wheelchair (DY611A-2, DY612A-1)
- Applicant
- Zhejiang Lumbre Electric Appliance Co., Ltd. CN
- Product code
- ITI — Wheelchair, Powered
- Decision date
- 2026-07-10
- Date received
- 2026-04-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K261149.pdf
Official FDA record: K261149
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.