K233789
- 510(k) number
- K233789
- Device name
- 8Q10 Surclear Smoke Plume Evacuation System
- Applicant
- Surnic Corporation CA · US
- Product code
- FYD — Apparatus, Exhaust, Surgical
- Decision date
- 2024-04-10
- Date received
- 2023-11-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K233789.pdf
Official FDA record: K233789
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.