PMA de la FDA

STENT, RENAL

Número de PMA: P060006 · 2023-12-12

SolicitanteBoston Scientific Corp

Fecha de decisión2023-12-12

Número PMAP060006

Código de productoNIN

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorCV

Resumen del dispositivo

STENT, RENAL is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2023-12-12. The device is classified under product code NIN. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the STENT, RENAL?

STENT, RENAL is a medical device that received FDA 510(k) clearance on 2023-12-12. The listed applicant is Boston Scientific Corp.

When did STENT, RENAL receive FDA 510(k) clearance?

The clearance date for STENT, RENAL can be found in the official FDA records.

Who is the listed applicant for STENT, RENAL?

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

What is the FDA product code for STENT, RENAL?

The FDA product code for STENT, RENAL is NIN.

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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.