K253777
- 510(k) number
- K253777
- Device name
- Ascblue (8010)
- Applicant
- Ascblue Corporation CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-04-10
- Date received
- 2025-11-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K253777.pdf
Official FDA record: K253777
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.