meddevicedb.com FDA Device Reference

IPL Hair Removal (Model: SL-B080, SL-B126, SL-B136)

K221246 Class II Traditional
Decision Date
2022-07-07
Sponsor / Applicant
Shenzhen Semlamp Intelligent Technology Co., Ltd.

Technical Specification

510(k) Submission ID K221246
Product Code OHT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2022-07-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IPL Hair Removal (Model: SL-B080, SL-B126, SL-B136) received FDA 510(k) clearance under submission number K221246, sponsored by Shenzhen Semlamp Intelligent Technology Co., 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 2022-07-07.

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.