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PMA de la FDA

Implantable pulse generator, pacemaker (non-CRT)

Número de PMA: P820003 · 2025-03-20

SolicitanteMedtronic Cardiac Rhythm Disease Management
Fecha de decisión2025-03-20
Número PMAP820003
Código de productoLWP
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Implantable pulse generator, pacemaker (non-CRT) is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Cardiac Rhythm Disease Management. It received FDA 510(k) clearance on 2025-03-20. The device is classified under product code LWP. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Implantable pulse generator, pacemaker (non-CRT)?

Implantable pulse generator, pacemaker (non-CRT) is a medical device that received FDA 510(k) clearance on 2025-03-20. The listed applicant is Medtronic Cardiac Rhythm Disease Management.

When did Implantable pulse generator, pacemaker (non-CRT) receive FDA 510(k) clearance?

The clearance date for Implantable pulse generator, pacemaker (non-CRT) can be found in the official FDA records.

Who is the listed applicant for Implantable pulse generator, pacemaker (non-CRT)?

The FDA 510(k) record lists Medtronic Cardiac Rhythm Disease Management as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Implantable pulse generator, pacemaker (non-CRT)?

The FDA product code for Implantable pulse generator, pacemaker (non-CRT) is LWP.

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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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