FDA 510(k)

MEDO ARIA

N.º K: K200356 · 2020-06-11

SolicitanteMedo.Ai

Fecha de decisión2020-06-11

Código de productoQIH

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

MEDO ARIA is the device name listed in this FDA 510(k) record. The listed applicant is Medo.Ai. It received FDA 510(k) clearance on 2020-06-11 under 510(k) number K200356. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the MEDO ARIA?

MEDO ARIA is a medical device that received FDA 510(k) clearance on 2020-06-11. The listed applicant is Medo.Ai. The 510(k) number is K200356.

When did MEDO ARIA receive FDA 510(k) clearance?

MEDO ARIA received FDA 510(k) clearance on 2020-06-11, under 510(k) number K200356.

Who is the listed applicant for MEDO ARIA?

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

What is the FDA product code for MEDO ARIA?

The FDA product code for MEDO ARIA is QIH.

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Fuente oficial

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