FDA 510(k)

Ventoux VC2; Ventoux VC3

Número K: K223120 · 2024-12-02

RequerenteFlight Medical Innovations , Ltd.

Data da decisão2024-12-02

Código do produtoCBK

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ventoux VC2; Ventoux VC3 is the device name listed in this FDA 510(k) record. The listed applicant is Flight Medical Innovations , Ltd.. It received FDA 510(k) clearance on 2024-12-02 under 510(k) number K223120. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Ventoux VC2; Ventoux VC3?

Ventoux VC2; Ventoux VC3 is a medical device that received FDA 510(k) clearance on 2024-12-02. The listed applicant is Flight Medical Innovations , Ltd.. The 510(k) number is K223120.

When did Ventoux VC2; Ventoux VC3 receive FDA 510(k) clearance?

Ventoux VC2; Ventoux VC3 received FDA 510(k) clearance on 2024-12-02, under 510(k) number K223120.

Who is the listed applicant for Ventoux VC2; Ventoux VC3?

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

What is the FDA product code for Ventoux VC2; Ventoux VC3?

The FDA product code for Ventoux VC2; Ventoux VC3 is CBK.

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Fonte oficial

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