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PMA de la FDA

Pulse-generator, single chamber, sensor driven, implantable

Número de PMA: P850051 · 2025-03-20

SolicitanteMedtronic, Inc.
Fecha de decisión2025-03-20
Número PMAP850051
Código de productoLWO
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Pulse-generator, single chamber, sensor driven, implantable is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2025-03-20. The device is classified under product code LWO. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Pulse-generator, single chamber, sensor driven, implantable?

Pulse-generator, single chamber, sensor driven, implantable is a medical device that received FDA 510(k) clearance on 2025-03-20. The listed applicant is Medtronic, Inc..

When did Pulse-generator, single chamber, sensor driven, implantable receive FDA 510(k) clearance?

The clearance date for Pulse-generator, single chamber, sensor driven, implantable can be found in the official FDA records.

Who is the listed applicant for Pulse-generator, single chamber, sensor driven, implantable?

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

What is the FDA product code for Pulse-generator, single chamber, sensor driven, implantable?

The FDA product code for Pulse-generator, single chamber, sensor driven, implantable is LWO.

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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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