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PMA de la FDA

Cardiac ablation percutaneous catheter

Número de PMA: P960016 · 2026-08-07

SolicitanteSt Jude Medical
Fecha de decisión2026-08-07
Número PMAP960016
Código de productoLPB
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Cardiac ablation percutaneous catheter is the device name listed in this FDA 510(k) record. The listed applicant is St Jude Medical. It received FDA 510(k) clearance on 2026-08-07. The device is classified under product code LPB. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Cardiac ablation percutaneous catheter?

Cardiac ablation percutaneous catheter is a medical device that received FDA 510(k) clearance on 2026-08-07. The listed applicant is St Jude Medical.

When did Cardiac ablation percutaneous catheter receive FDA 510(k) clearance?

The clearance date for Cardiac ablation percutaneous catheter can be found in the official FDA records.

Who is the listed applicant for Cardiac ablation percutaneous catheter?

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

What is the FDA product code for Cardiac ablation percutaneous catheter?

The FDA product code for Cardiac ablation percutaneous catheter is LPB.

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Fuente oficial

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