meddevicedb.com FDA Device Reference

Hair Growth Device (KCA441-200, KCA441-120, KCA441-88, KCA441-56, KCA441-200S, KCA441-120S, KCA441-88S, KCA441-56S, KCA451-200, KCA451-120, KCA451-88, KCA451-56, KCA451-200S, KCA451-120S, KCA451-88S, KCA451-56S)

K250308 Class II Traditional
Decision Date
2025-04-29
Sponsor / Applicant
Dongguan Boyuan Intelligent Technology Co.,Ltd

Technical Specification

510(k) Submission ID K250308
Product Code OAP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2025-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hair Growth Device (KCA441-200, KCA441-120, KCA441-88, KCA441-56, KCA441-200S, KCA441-120S, KCA441-88S, KCA441-56S, KCA451-200, KCA451-120, KCA451-88, KCA451-56, KCA451-200S, KCA451-120S, KCA451-88S, KCA451-56S) received FDA 510(k) clearance under submission number K250308, sponsored by Dongguan Boyuan Intelligent 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 2025-04-29.

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.