K240267
- 510(k) number
- K240267
- Device name
- Klaxon (Twist); Klaxon (Twist R)
- Applicant
- Klaxon Mobility GmbH AT
- Product code
- ITI — Wheelchair, Powered
- Decision date
- 2025-01-10
- Date received
- 2024-01-31
- 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: K240267.pdf
Official FDA record: K240267
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.