K250852
- 510(k) number
- K250852
- Device name
- Coolfase
- Applicant
- Asterasys Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-10-16
- Date received
- 2025-03-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K250852.pdf
Official FDA record: K250852
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.