meddevicedb.com FDA Device Reference

PLUME-AWAY SMOKE EVACUATION SYSTEM

K894038 Class II Traditional
Decision Date
1989-09-28
Sponsor / Applicant
Laser Technologies Group, Inc.

Technical Specification

510(k) Submission ID K894038
Product Code FYD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5070
Decision Date 1989-09-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLUME-AWAY SMOKE EVACUATION SYSTEM received FDA 510(k) clearance under submission number K894038, sponsored by Laser Technologies Group, Inc.. 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 1989-09-28.

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.