meddevicedb.com FDA Device Reference

micro IPL

K172181 Class II Traditional
Decision Date
2017-10-13
Sponsor / Applicant
El Global Trade, Ltd.

Technical Specification

510(k) Submission ID K172181
Product Code OHT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2017-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

micro IPL received FDA 510(k) clearance under submission number K172181, sponsored by El Global Trade, 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 2017-10-13.

Classification & Regulation

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