K250657
- 510(k) number
- K250657
- Device name
- gi2000 Electrosurgical Generator
- Applicant
- Cintron Medical Corporation CO · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-06-03
- Date received
- 2025-03-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K250657.pdf
Official FDA record: K250657
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.