K260937

Smart Electric Wheelchair (R1-Std-BK, R1-Pro-BK, R1-Ultra-GK, R1-Ultra-WK)

510(k) number
K260937
Device name
Smart Electric Wheelchair (R1-Std-BK, R1-Pro-BK, R1-Ultra-GK, R1-Ultra-WK)
Applicant
Shanghai Waylong Intelligent Technology Co.,Ltd CN
Product code
ITI — Wheelchair, Powered
Decision date
2026-06-24
Date received
2026-03-20
Decision
Substantially Equivalent
Clearance type
Traditional
Advisory committee
Physical Medicine
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain

Also available from FDA: K260937.pdf

Official FDA record: K260937
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.