meddevicedb.com FDA Device Reference

8Q10 Surclear Smoke Plume Evacuation System

K233789 Class II Traditional
Decision Date
2024-04-10
Sponsor / Applicant
Surnic Corporation

Technical Specification

510(k) Submission ID K233789
Product Code FYD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5070
Decision Date 2024-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

8Q10 Surclear Smoke Plume Evacuation System received FDA 510(k) clearance under submission number K233789, sponsored by Surnic Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code FYD and 21 CFR 878.5070, within the General, Plastic Surgery review panel as a Class II device.