K250841
- 510(k) number
- K250841
- Device name
- Electrotherapy Electrodes
- Applicant
- Baisheng Medical Co., Ltd. CN
- Product code
- GXY — Electrode, Cutaneous
- Decision date
- 2025-08-13
- Date received
- 2025-03-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K250841.pdf
Official FDA record: K250841
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.