K252833
- 510(k) number
- K252833
- Device name
- VIVA combo RF System
- Applicant
- Starmed Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-05-26
- Date received
- 2025-09-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K252833.pdf
Official FDA record: K252833
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.