Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EMS Neck Massager

K-Number: K233492 · 2023-12-20

ApplicantXiamen Comfier Technology Co., Ltd.
Decision Date2023-12-20
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EMS Neck Massager is a medical device manufactured by Xiamen Comfier Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-12-20 under approval number K233492. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMS Neck Massager?

EMS Neck Massager is a medical device that received FDA 510(k) clearance on 2023-12-20. It is manufactured by Xiamen Comfier Technology Co., Ltd.. The 510(k) number is K233492.

When was EMS Neck Massager approved by the FDA?

EMS Neck Massager received FDA 510(k) clearance on 2023-12-20, under approval number K233492.

What company makes EMS Neck Massager?

EMS Neck Massager is manufactured by Xiamen Comfier Technology Co., Ltd..

What is the FDA product code for EMS Neck Massager?

The FDA product code for EMS Neck Massager is NGX.

Related Devices (Code: NGX)

K152420AK Body Toning DeviceAk Beauty Enterprises, LLC K161974SLENDERTONE® Connect Abs, Type 570Bio-Medical Research, Ltd. K152480Revitive Medic; Revitive MV; Revitive LVActegy , Ltd. K151722Slim UP ULTRAAime Medical, Inc. K172876PowerDot PD-01MSmartmissimo Technologies Pte, Ltd. K172241Tyece OTC EMS System, Model EM35Tyece , Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑