meddevicedb.com FDA Device Reference

IPL Hair Removal Device (M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023)

K250131 Class II Traditional
Decision Date
2025-03-19
Sponsor / Applicant
Mustech Electronics Co., Limited

Technical Specification

510(k) Submission ID K250131
Product Code OHT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2025-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IPL Hair Removal Device (M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023) received FDA 510(k) clearance under submission number K250131, sponsored by Mustech Electronics Co., Limited. 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 2025-03-19.

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.