Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)
K-Number: K201845 · 2020-10-08
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.