K261175
- 510(k) number
- K261175
- Device name
- WHILL (WHILL Model C2)
- Applicant
- Whill, Inc. JP
- Product code
- ITI — Wheelchair, Powered
- Decision date
- 2026-06-12
- Date received
- 2026-04-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K261175.pdf
Official FDA record: K261175
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.