FDA 510(k)

Sheridan Endobronchial Tubes

N.º K: K180253 · 2018-11-02

Fecha de decisión2018-11-02

Código de productoCBI

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del dispositivo

Sheridan Endobronchial Tubes is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2018-11-02 under 510(k) number K180253. 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 Sheridan Endobronchial Tubes?

Sheridan Endobronchial Tubes is a medical device that received FDA 510(k) clearance on 2018-11-02. The listed applicant is Teleflex Medical. The 510(k) number is K180253.

When did Sheridan Endobronchial Tubes receive FDA 510(k) clearance?

Sheridan Endobronchial Tubes received FDA 510(k) clearance on 2018-11-02, under 510(k) number K180253.

Who is the listed applicant for Sheridan Endobronchial Tubes?

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

What is the FDA product code for Sheridan Endobronchial Tubes?

The FDA product code for Sheridan Endobronchial Tubes is CBI.

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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.