meddevicedb.com FDA Device Reference

LASER GAS MIXTURE

K935034 Class II Traditional
Decision Date
1993-12-14
Sponsor / Applicant
Tri-Gas, Inc.

Technical Specification

510(k) Submission ID K935034
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1993-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LASER GAS MIXTURE received FDA 510(k) clearance under submission number K935034, sponsored by Tri-Gas, 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 1993-12-14.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.