meddevicedb.com FDA Device Reference

Hand Massager (SM004D)

K251622 Class II Traditional
Decision Date
2026-01-28
Sponsor / Applicant
Ningbo Zhenhai Yihao Electronic Technology Co., Ltd.

Technical Specification

510(k) Submission ID K251622
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2026-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hand Massager (SM004D) received FDA 510(k) clearance under submission number K251622, sponsored by Ningbo Zhenhai Yihao Electronic 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 2026-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code IRP and 21 CFR 890.5650, within the Physical Medicine review panel as a Class II device.