meddevicedb.com FDA Device Reference

Q-PLUS T+ IPL LASER SYSTEM

K123168 Class II Traditional
Decision Date
2012-12-20
Sponsor / Applicant
Quanta System Spa

Technical Specification

510(k) Submission ID K123168
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2012-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Q-PLUS T+ IPL LASER SYSTEM received FDA 510(k) clearance under submission number K123168, sponsored by Quanta System Spa. 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 2012-12-20.

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.