meddevicedb.com FDA Device Reference

Hair Growth System

K191754 Class II Traditional
Decision Date
2019-11-22
Sponsor / Applicant
Kunshan Bella Optical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K191754
Product Code OAP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2019-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hair Growth System received FDA 510(k) clearance under submission number K191754, sponsored by Kunshan Bella Optical Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2019-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code OAP and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.