FDA 510(k)

JOVS Electric Stimulation Beauty Device (JE2)

N.º K: K250227 · 2025-10-17

SolicitanteShenzhen Qianyu Technology Co., Ltd.

Fecha de decisión2025-10-17

Código de productoNFO

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

JOVS Electric Stimulation Beauty Device (JE2) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Qianyu Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-10-17 under 510(k) number K250227. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the JOVS Electric Stimulation Beauty Device (JE2)?

JOVS Electric Stimulation Beauty Device (JE2) is a medical device that received FDA 510(k) clearance on 2025-10-17. The listed applicant is Shenzhen Qianyu Technology Co., Ltd.. The 510(k) number is K250227.

When did JOVS Electric Stimulation Beauty Device (JE2) receive FDA 510(k) clearance?

JOVS Electric Stimulation Beauty Device (JE2) received FDA 510(k) clearance on 2025-10-17, under 510(k) number K250227.

Who is the listed applicant for JOVS Electric Stimulation Beauty Device (JE2)?

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

What is the FDA product code for JOVS Electric Stimulation Beauty Device (JE2)?

The FDA product code for JOVS Electric Stimulation Beauty Device (JE2) is NFO.

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Otros registros que enlistan a Shenzhen Qianyu Technology Co., Ltd. como solicitante

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Fuente oficial

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