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PMA de la FDA

Intravascular radiation delivery system

Número de PMA: P000018 · 2024-09-26

SolicitanteBest Vascular, Inc.
Fecha de decisión2024-09-26
Número PMAP000018
Código de productoMOU
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Intravascular radiation delivery system is the device name listed in this FDA 510(k) record. The listed applicant is Best Vascular, Inc.. It received FDA 510(k) clearance on 2024-09-26. The device is classified under product code MOU. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Intravascular radiation delivery system?

Intravascular radiation delivery system is a medical device that received FDA 510(k) clearance on 2024-09-26. The listed applicant is Best Vascular, Inc..

When did Intravascular radiation delivery system receive FDA 510(k) clearance?

The clearance date for Intravascular radiation delivery system can be found in the official FDA records.

Who is the listed applicant for Intravascular radiation delivery system?

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

What is the FDA product code for Intravascular radiation delivery system?

The FDA product code for Intravascular radiation delivery system is MOU.

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Fuente oficial

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