meddevicedb.com FDA Device Reference

TWO SKIN TREATMENT SYSTEM

K141507 Class II Traditional
Decision Date
2014-12-08
Sponsor / Applicant
Syneron Medical, Ltd.

Technical Specification

510(k) Submission ID K141507
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2014-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TWO SKIN TREATMENT SYSTEM received FDA 510(k) clearance under submission number K141507, sponsored by Syneron Medical, Ltd.. 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 2014-12-08.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.