K240975
- 510(k) number
- K240975
- Device name
- Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300)
- Applicant
- Beijing Taktvoll Technology Co., Ltd. CN
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-12-23
- Date received
- 2024-04-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K240975.pdf
Official FDA record: K240975
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.