K251836
- 510(k) number
- K251836
- Device name
- Dermatrix Duo
- Applicant
- Shenzhen Gsd Technology Co., Ltd. CN
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-02-06
- Date received
- 2025-06-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251836.pdf
Official FDA record: K251836
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.