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VISUALASE THERMAL THERAPY SYSTEM

K071328 Class II Traditional
Decision Date
2007-08-31
Sponsor / Applicant
Biotex, Inc.

Technical Specification

510(k) Submission ID K071328
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2007-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISUALASE THERMAL THERAPY SYSTEM received FDA 510(k) clearance under submission number K071328, sponsored by Biotex, 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 2007-08-31.

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.