PMA de la FDA

Stent, carotid

Número de PMA: P180010 · 2019-03-18

SolicitanteW. L. Gore & Associates, Inc.

Fecha de decisión2019-03-18

Número PMAP180010

Código de productoNIM

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorCV

Resumen del dispositivo

Stent, carotid is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Gore & Associates, Inc.. It received FDA 510(k) clearance on 2019-03-18. The device is classified under product code NIM. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Stent, carotid?

Stent, carotid is a medical device that received FDA 510(k) clearance on 2019-03-18. The listed applicant is W. L. Gore & Associates, Inc..

When did Stent, carotid receive FDA 510(k) clearance?

The clearance date for Stent, carotid can be found in the official FDA records.

Who is the listed applicant for Stent, carotid?

The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stent, carotid?

The FDA product code for Stent, carotid is NIM.

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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.