meddevicedb.com FDA Device Reference

ILUMINAGE SKIN SMOOTHING LASER

K133473 Class II Special
Decision Date
2014-01-15
Sponsor / Applicant
Cynosure, Inc.

Technical Specification

510(k) Submission ID K133473
Product Code OHS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2014-01-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ILUMINAGE SKIN SMOOTHING LASER received FDA 510(k) clearance under submission number K133473, sponsored by Cynosure, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2014-01-15.

Classification & Regulation

This clearance is catalogued under FDA product code OHS and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.