FDA 510(k)

Portable Electro-Stimulation Therapy Device

N.º K: K182108 · 2019-04-26

SolicitanteGuangzhou Longest Science & Technology Co., Ltd.

Fecha de decisión2019-04-26

Código de productoNUH

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Portable Electro-Stimulation Therapy Device is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Longest Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2019-04-26 under 510(k) number K182108. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Portable Electro-Stimulation Therapy Device?

Portable Electro-Stimulation Therapy Device is a medical device that received FDA 510(k) clearance on 2019-04-26. The listed applicant is Guangzhou Longest Science & Technology Co., Ltd.. The 510(k) number is K182108.

When did Portable Electro-Stimulation Therapy Device receive FDA 510(k) clearance?

Portable Electro-Stimulation Therapy Device received FDA 510(k) clearance on 2019-04-26, under 510(k) number K182108.

Who is the listed applicant for Portable Electro-Stimulation Therapy Device?

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

What is the FDA product code for Portable Electro-Stimulation Therapy Device?

The FDA product code for Portable Electro-Stimulation Therapy Device is NUH.

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Otros registros que enlistan a Guangzhou Longest Science & Technology Co., Ltd. como solicitante

K202110MStim Drop Model: LGT-233 K201845Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)K182020Portable Electro-Stimulation Therapy Device K191856Compression Therapy Device K191862Compression Therapy Device Model LGT-2200SP

Dispositivos relacionados (Código: NUH)

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