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PMA de la FDA

Ventricular (assist) bypass

Número de PMA: P170038 · 2026-09-02

SolicitanteAbbott
Fecha de decisión2026-09-02
Número PMAP170038
Código de productoDSQ
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Ventricular (assist) bypass is the device name listed in this FDA 510(k) record. The listed applicant is Abbott. It received FDA 510(k) clearance on 2026-09-02. The device is classified under product code DSQ. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Ventricular (assist) bypass?

Ventricular (assist) bypass is a medical device that received FDA 510(k) clearance on 2026-09-02. The listed applicant is Abbott.

When did Ventricular (assist) bypass receive FDA 510(k) clearance?

The clearance date for Ventricular (assist) bypass can be found in the official FDA records.

Who is the listed applicant for Ventricular (assist) bypass?

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

What is the FDA product code for Ventricular (assist) bypass?

The FDA product code for Ventricular (assist) bypass is DSQ.

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Fuente oficial

Ver en la base de datos de la FDA →

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