FDA 510(k)

Ambu VivaSight 2 DLT, Cable Adaptador Ambu VivaSight 2

N.º K: K203749 · 2021-05-03

Fecha de decisión2021-05-03

Código de productoCBI

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del dispositivo

Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable is the device name listed in this FDA 510(k) record. The listed applicant is Ambu A/S. It received FDA 510(k) clearance on 2021-05-03 under 510(k) number K203749. The device is classified under product code CBI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable?

Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable is a medical device that received FDA 510(k) clearance on 2021-05-03. The listed applicant is Ambu A/S. The 510(k) number is K203749.

When did Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable receive FDA 510(k) clearance?

Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable received FDA 510(k) clearance on 2021-05-03, under 510(k) number K203749.

Who is the listed applicant for Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable?

The FDA 510(k) record lists Ambu A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable?

The FDA product code for Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable is CBI.

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Otros registros que enlistan a Ambu A/S como solicitante

K260309Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler Set K261400Ambu® aScope™ Gastro; Ambu® aScope™ Gastro Large K260578Ambu® NeurolineTM Copa MRI/CT (Modelos 72704/21US, 72704/23US, 72704/25US, 72704/27US) Ambu® NeurolineTM Copa MRI/CT-set (Modelos 72704/21-1010US, 72704/21-1010US, 72704/23-1010US, 72704/25-1010US, 72704/27-1010US) Ambu® NeurolineTM Copa MRI/CT-mini set (Modelos 72704/21-0301US, 72704/23-0301US, 72704/25-0301US, 72704/27-0301US)K251583Filtro de Exhalación Ambu® Virobac II®K250269Ambu® aScope™ 5 Cysto HD (Standard Deflection); Ambu® aScope™ 5 Cysto HD (Reverse Deflection)K240849Ambu® aScope™ 5 Cysto HD (Desviación Estándar); Ambu® aScope™ 5 Cysto HD (Desviación Inversa); Ambu® aBox™ 2

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Dispositivos relacionados (Código: CBI)

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.