meddevicedb.com FDA Device Reference

Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil

K170721 Class II Traditional
Decision Date
2017-04-21
Sponsor / Applicant
Precision Surgical, LLC

Technical Specification

510(k) Submission ID K170721
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2017-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cut-Vac Lighted Smoke Evacuation Electrosurgical Pencil received FDA 510(k) clearance under submission number K170721, sponsored by Precision Surgical, LLC. 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 2017-04-21.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.