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PMA de la FDA

Ablation catheter, renal denervation

Número de PMA: P220023 · 2026-08-13

SolicitanteRecor Medical, Inc.
Fecha de decisión2026-08-13
Número PMAP220023
Código de productoQYI
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Ablation catheter, renal denervation is the device name listed in this FDA 510(k) record. The listed applicant is Recor Medical, Inc.. It received FDA 510(k) clearance on 2026-08-13. The device is classified under product code QYI. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Ablation catheter, renal denervation?

Ablation catheter, renal denervation is a medical device that received FDA 510(k) clearance on 2026-08-13. The listed applicant is Recor Medical, Inc..

When did Ablation catheter, renal denervation receive FDA 510(k) clearance?

The clearance date for Ablation catheter, renal denervation can be found in the official FDA records.

Who is the listed applicant for Ablation catheter, renal denervation?

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

What is the FDA product code for Ablation catheter, renal denervation?

The FDA product code for Ablation catheter, renal denervation is QYI.

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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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