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PMA de la FDA

Stimulator, electrical, implanted, for parkinsonian symptoms

Número de PMA: P150031 · 2026-09-22

SolicitanteBoston Scientific Corp
Fecha de decisión2026-09-22
Número PMAP150031
Código de productoNHL
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorNE

Resumen del dispositivo

Stimulator, electrical, implanted, for parkinsonian symptoms 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 2026-09-22. The device is classified under product code NHL. It was reviewed by the NE advisory panel.

Preguntas frecuentes

What is the Stimulator, electrical, implanted, for parkinsonian symptoms?

Stimulator, electrical, implanted, for parkinsonian symptoms is a medical device that received FDA 510(k) clearance on 2026-09-22. The listed applicant is Boston Scientific Corp.

When did Stimulator, electrical, implanted, for parkinsonian symptoms receive FDA 510(k) clearance?

The clearance date for Stimulator, electrical, implanted, for parkinsonian symptoms can be found in the official FDA records.

Who is the listed applicant for Stimulator, electrical, implanted, for parkinsonian symptoms?

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 Stimulator, electrical, implanted, for parkinsonian symptoms?

The FDA product code for Stimulator, electrical, implanted, for parkinsonian symptoms is NHL.

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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.

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