K262654
- 510(k) number
- K262654
- Device name
- Dexus Prosthetic System (MSL2, MSR2)
- Applicant
- Zhejiang Qiangnao Technology Co.,Ltd CN
- Product code
- GXY — Electrode, Cutaneous
- Decision date
- 2026-08-27
- Date received
- 2026-07-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K262654.pdf
Official FDA record: K262654
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.