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FDA 510(k)

Auxo A300, A150 and APod

N.º K: K220543 · 2022-04-20

SolicitanteAuxo Hair, LLC
Fecha de decisión2022-04-20
Código de productoOAP
Comité asesorPM
DecisiónSubstantially Equivalent

Resumen del dispositivo

Auxo A300, A150 and APod is the device name listed in this FDA 510(k) record. The listed applicant is Auxo Hair, LLC. It received FDA 510(k) clearance on 2022-04-20 under 510(k) number K220543. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Auxo A300, A150 and APod?

Auxo A300, A150 and APod is a medical device that received FDA 510(k) clearance on 2022-04-20. The listed applicant is Auxo Hair, LLC. The 510(k) number is K220543.

When did Auxo A300, A150 and APod receive FDA 510(k) clearance?

Auxo A300, A150 and APod received FDA 510(k) clearance on 2022-04-20, under 510(k) number K220543.

Who is the listed applicant for Auxo A300, A150 and APod?

The FDA 510(k) record lists Auxo Hair, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Auxo A300, A150 and APod?

The FDA product code for Auxo A300, A150 and APod is OAP.

Dispositivos relacionados (Código: OAP)

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Fuente oficial

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