K232193
- 510(k) number
- K232193
- Device name
- Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)
- Applicant
- Yurob Rehabilitation Medical Co., Ltd. CN
- Product code
- ITI — Wheelchair, Powered
- Decision date
- 2023-09-22
- Date received
- 2023-07-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K232193.pdf
Official FDA record: K232193
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.