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FDA 510(k)

Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)

K-Number: K201845 · 2020-10-08

Decision Date2020-10-08
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Portable Electro-Stimulation Therapy Device, Model: LGT-232(US) is a medical device manufactured by Guangzhou Longest Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-10-08 under approval number K201845. 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 Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)?

Portable Electro-Stimulation Therapy Device, Model: LGT-232(US) is a medical device that received FDA 510(k) clearance on 2020-10-08. It is manufactured by Guangzhou Longest Science & Technology Co., Ltd.. The 510(k) number is K201845.

When was Portable Electro-Stimulation Therapy Device, Model: LGT-232(US) approved by the FDA?

Portable Electro-Stimulation Therapy Device, Model: LGT-232(US) received FDA 510(k) clearance on 2020-10-08, under approval number K201845.

What company makes Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)?

Portable Electro-Stimulation Therapy Device, Model: LGT-232(US) is manufactured by Guangzhou Longest Science & Technology Co., Ltd..

What is the FDA product code for Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)?

The FDA product code for Portable Electro-Stimulation Therapy Device, Model: LGT-232(US) is NGX.

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Official Source

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