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FDA 510(k)

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1

N.º K: K250361 · 2025-05-23

SolicitanteGeske Beauty Tech GmbH
Fecha de decisión2025-05-23
Código de productoNFO
Comité asesorNE
DecisiónSubstantially Equivalent

Resumen del dispositivo

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is the device name listed in this FDA 510(k) record. The listed applicant is Geske Beauty Tech GmbH. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K250361. 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 SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Geske Beauty Tech GmbH. The 510(k) number is K250361.

When did SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 receive FDA 510(k) clearance?

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 received FDA 510(k) clearance on 2025-05-23, under 510(k) number K250361.

Who is the listed applicant for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

The FDA 510(k) record lists Geske Beauty Tech GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

The FDA product code for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is NFO.

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Fuente oficial

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