FDA 510(k)

V80 Anesthetic Vaporizer (V80)

N.º K: K240375 · 2024-10-31

SolicitanteShenzhen Mindray Bio-Medical Electronics Co., Ltd.

Fecha de decisión2024-10-31

Código de productoCAD

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del dispositivo

V80 Anesthetic Vaporizer (V80) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2024-10-31 under 510(k) number K240375. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the V80 Anesthetic Vaporizer (V80)?

V80 Anesthetic Vaporizer (V80) is a medical device that received FDA 510(k) clearance on 2024-10-31. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K240375.

When did V80 Anesthetic Vaporizer (V80) receive FDA 510(k) clearance?

V80 Anesthetic Vaporizer (V80) received FDA 510(k) clearance on 2024-10-31, under 510(k) number K240375.

Who is the listed applicant for V80 Anesthetic Vaporizer (V80)?

The FDA 510(k) record lists Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V80 Anesthetic Vaporizer (V80)?

The FDA product code for V80 Anesthetic Vaporizer (V80) is CAD.

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Otros registros que enlistan a Shenzhen Mindray Bio-Medical Electronics Co., Ltd. como solicitante

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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.