meddevicedb.com FDA Device Reference

EMS Neck Massager

K233492 Class II Traditional
Decision Date
2023-12-20
Sponsor / Applicant
Xiamen Comfier Technology Co., Ltd.

Technical Specification

510(k) Submission ID K233492
Product Code NGX
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2023-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMS Neck Massager received FDA 510(k) clearance under submission number K233492, sponsored by Xiamen Comfier 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 2023-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code NGX and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.