FDA 510(k)

Nooro Body & Foot Stimulator (SM9141, SM9142)

N.º K: K243334 · 2024-11-22

Fecha de decisión2024-11-22

Código de productoNUH

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Nooro Body & Foot Stimulator (SM9141, SM9142) is the device name listed in this FDA 510(k) record. The listed applicant is Xf Agencija Limited. It received FDA 510(k) clearance on 2024-11-22 under 510(k) number K243334. 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 Nooro Body & Foot Stimulator (SM9141, SM9142)?

Nooro Body & Foot Stimulator (SM9141, SM9142) is a medical device that received FDA 510(k) clearance on 2024-11-22. The listed applicant is Xf Agencija Limited. The 510(k) number is K243334.

When did Nooro Body & Foot Stimulator (SM9141, SM9142) receive FDA 510(k) clearance?

Nooro Body & Foot Stimulator (SM9141, SM9142) received FDA 510(k) clearance on 2024-11-22, under 510(k) number K243334.

Who is the listed applicant for Nooro Body & Foot Stimulator (SM9141, SM9142)?

The FDA 510(k) record lists Xf Agencija Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nooro Body & Foot Stimulator (SM9141, SM9142)?

The FDA product code for Nooro Body & Foot Stimulator (SM9141, SM9142) is NUH.

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Fuente oficial

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