K251334
- 510(k) number
- K251334
- Device name
- NEW DOUBLO 2.0
- Applicant
- Hironic Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-09-29
- Date received
- 2025-04-30
- 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: K251334.pdf
Official FDA record: K251334
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.