FDA 510(k)

INNI-CERA

N.º K: K211308 · 2021-10-04

Fecha de decisión2021-10-04

Código de productoEIH

Comité asesorDE

DecisiónSubstantially Equivalent

Resumen del dispositivo

INNI-CERA is the device name listed in this FDA 510(k) record. The listed applicant is Aon Co., Ltd.. It received FDA 510(k) clearance on 2021-10-04 under 510(k) number K211308. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the INNI-CERA?

INNI-CERA is a medical device that received FDA 510(k) clearance on 2021-10-04. The listed applicant is Aon Co., Ltd.. The 510(k) number is K211308.

When did INNI-CERA receive FDA 510(k) clearance?

INNI-CERA received FDA 510(k) clearance on 2021-10-04, under 510(k) number K211308.

Who is the listed applicant for INNI-CERA?

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

What is the FDA product code for INNI-CERA?

The FDA product code for INNI-CERA is EIH.

Dispositivos relacionados (Código: EIH)

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.