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FDA 510(k)

EMS Neck Massager

K-Number: K233492 · 2023-12-20

Decision Date2023-12-20
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EMS Neck Massager is the device name listed in this FDA 510(k) record. The listed applicant is Xiamen Comfier Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-12-20 under 510(k) 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. The listed applicant is Xiamen Comfier Technology Co., Ltd.. The 510(k) number is K233492.

When did EMS Neck Massager receive FDA 510(k) clearance?

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

Who is the listed applicant for EMS Neck Massager?

The FDA 510(k) record lists Xiamen Comfier Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMS Neck Massager?

The FDA product code for EMS Neck Massager is NGX.

Related Devices (Code: NGX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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