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LIGHT-TOUCH AND SURGI LIGHT FIBERS

K910726 Class II Traditional
Decision Date
1991-03-29
Sponsor / Applicant
Lifestream Int'L, Inc.

Technical Specification

510(k) Submission ID K910726
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1991-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIGHT-TOUCH AND SURGI LIGHT FIBERS received FDA 510(k) clearance under submission number K910726, sponsored by Lifestream Int'L, 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 1991-03-29.

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.