K241460
- 510(k) number
- K241460
- Device name
- Manual Wheelchair
- Applicant
- Lichtmega Technology Co., Ltd. CN
- Product code
- IOR — Wheelchair, Mechanical
- Decision date
- 2024-07-11
- Date received
- 2024-05-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.2 MB · U.S. public domain
Also available from FDA: K241460.pdf
Official FDA record: K241460
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.