K241512
- 510(k) number
- K241512
- Device name
- Electrode Pad
- Applicant
- Shenzhen Deliduo Medical Technology Co.,Ltd CN
- Product code
- GXY — Electrode, Cutaneous
- Decision date
- 2025-01-15
- Date received
- 2024-05-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241512.pdf
Official FDA record: K241512
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.