meddevicedb.com FDA Device Reference

MEDICAL LASER MIXTURE

K935310 Class II Traditional
Decision Date
1993-12-23
Sponsor / Applicant
Acetylene Gas Co.

Technical Specification

510(k) Submission ID K935310
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1993-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDICAL LASER MIXTURE received FDA 510(k) clearance under submission number K935310, sponsored by Acetylene Gas Co.. 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 1993-12-23.

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.