meddevicedb.com FDA Device Reference

THREE-COMPONENT MEDICAL LASER GAS MIXTURES

K882516 Class II Traditional
Decision Date
1988-08-03
Sponsor / Applicant
Matheson Gas Products, Inc.

Technical Specification

510(k) Submission ID K882516
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1988-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THREE-COMPONENT MEDICAL LASER GAS MIXTURES received FDA 510(k) clearance under submission number K882516, sponsored by Matheson Gas Products, 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 1988-08-03.

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.