K243442
- 510(k) number
- K243442
- Device name
- iBOT® PMD
- Applicant
- Mobius Mobility NH · US
- Product code
- IMK — Wheelchair, Stair Climbing
- Decision date
- 2025-01-30
- Date received
- 2024-11-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K243442.pdf
Official FDA record: K243442
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.