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FDA 510(k)

Cary

N.º K: K251111 · 2025-05-07

SolicitanteExcitus AS
Fecha de decisión2025-05-07
Código de productoJCX
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Cary is the device name listed in this FDA 510(k) record. The listed applicant is Excitus AS. It received FDA 510(k) clearance on 2025-05-07 under 510(k) number K251111. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Cary?

Cary is a medical device that received FDA 510(k) clearance on 2025-05-07. The listed applicant is Excitus AS. The 510(k) number is K251111.

When did Cary receive FDA 510(k) clearance?

Cary received FDA 510(k) clearance on 2025-05-07, under 510(k) number K251111.

Who is the listed applicant for Cary?

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

What is the FDA product code for Cary?

The FDA product code for Cary is JCX.

Dispositivos relacionados (Código: JCX)

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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.

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