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FDA 510(k)

Wireless Pain Relieve Device

K-Number: K180331 · 2018-06-22

ApplicantShenzhen Dongdixin Technology Co., Ltd.
Decision Date2018-06-22
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Wireless Pain Relieve Device is a medical device manufactured by Shenzhen Dongdixin Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-06-22 under approval number K180331. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Wireless Pain Relieve Device?

Wireless Pain Relieve Device is a medical device that received FDA 510(k) clearance on 2018-06-22. It is manufactured by Shenzhen Dongdixin Technology Co., Ltd.. The 510(k) number is K180331.

When was Wireless Pain Relieve Device approved by the FDA?

Wireless Pain Relieve Device received FDA 510(k) clearance on 2018-06-22, under approval number K180331.

What company makes Wireless Pain Relieve Device?

Wireless Pain Relieve Device is manufactured by Shenzhen Dongdixin Technology Co., Ltd..

What is the FDA product code for Wireless Pain Relieve Device?

The FDA product code for Wireless Pain Relieve Device is NUH.

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Other Devices by Shenzhen Dongdixin Technology Co., Ltd.

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Related Devices (Code: NUH)

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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.

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