K234140
- 510(k) number
- K234140
- Device name
- VIVA combo RF System (VIVA combo RF System)
- Applicant
- Starmed Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-01-30
- Date received
- 2023-12-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K234140.pdf
Official FDA record: K234140
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.