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PMA de la FDA

Transvenous temporary phrenic nerve stimulator

Número de PMA: P240012 · 2026-09-25

SolicitanteLungpacer Medical USA, Inc.
Fecha de decisión2026-09-25
Número PMAP240012
Código de productoSDL
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorAN

Resumen del dispositivo

Transvenous temporary phrenic nerve stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Lungpacer Medical USA, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code SDL. It was reviewed by the AN advisory panel.

Preguntas frecuentes

What is the Transvenous temporary phrenic nerve stimulator?

Transvenous temporary phrenic nerve stimulator is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Lungpacer Medical USA, Inc..

When did Transvenous temporary phrenic nerve stimulator receive FDA 510(k) clearance?

The clearance date for Transvenous temporary phrenic nerve stimulator can be found in the official FDA records.

Who is the listed applicant for Transvenous temporary phrenic nerve stimulator?

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

What is the FDA product code for Transvenous temporary phrenic nerve stimulator?

The FDA product code for Transvenous temporary phrenic nerve stimulator is SDL.

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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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