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FDA 510(k)

Wireless Pain Relieve Device Model: LT5018C

K-Number: K173462 · 2017-12-08

ApplicantShenzhen Dongdixin Technology Co., Ltd.
Decision Date2017-12-08
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Wireless Pain Relieve Device Model: LT5018C is a medical device manufactured by Shenzhen Dongdixin Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-12-08 under approval number K173462. 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 Model: LT5018C?

Wireless Pain Relieve Device Model: LT5018C is a medical device that received FDA 510(k) clearance on 2017-12-08. It is manufactured by Shenzhen Dongdixin Technology Co., Ltd.. The 510(k) number is K173462.

When was Wireless Pain Relieve Device Model: LT5018C approved by the FDA?

Wireless Pain Relieve Device Model: LT5018C received FDA 510(k) clearance on 2017-12-08, under approval number K173462.

What company makes Wireless Pain Relieve Device Model: LT5018C?

Wireless Pain Relieve Device Model: LT5018C is manufactured by Shenzhen Dongdixin Technology Co., Ltd..

What is the FDA product code for Wireless Pain Relieve Device Model: LT5018C?

The FDA product code for Wireless Pain Relieve Device Model: LT5018C is NUH.

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Other Devices by Shenzhen Dongdixin Technology Co., Ltd.

K161735Non-contact Forehead Thermometer K171978Combo Stimulator MT9000, Combo Stimulator LT7102, TENS Stimulator InTENSity 10 K162479Smart Pain Reliever, Model LT5019 K180331Wireless Pain Relieve Device K171430Incontinence Treatment Device, Model LT2061 K210364Migraine Tens Digital Pain Reliever

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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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