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PMA de la FDA

Drug-eluting percutaneous transluminal coronary angioplasty catheter

Número de PMA: P250041 · 2026-09-18

SolicitanteMedAlliance, LLC
Fecha de decisión2026-09-18
Número PMAP250041
Código de productoOOB
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Drug-eluting percutaneous transluminal coronary angioplasty catheter is the device name listed in this FDA 510(k) record. The listed applicant is MedAlliance, LLC. It received FDA 510(k) clearance on 2026-09-18. The device is classified under product code OOB. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Drug-eluting percutaneous transluminal coronary angioplasty catheter?

Drug-eluting percutaneous transluminal coronary angioplasty catheter is a medical device that received FDA 510(k) clearance on 2026-09-18. The listed applicant is MedAlliance, LLC.

When did Drug-eluting percutaneous transluminal coronary angioplasty catheter receive FDA 510(k) clearance?

The clearance date for Drug-eluting percutaneous transluminal coronary angioplasty catheter can be found in the official FDA records.

Who is the listed applicant for Drug-eluting percutaneous transluminal coronary angioplasty catheter?

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

What is the FDA product code for Drug-eluting percutaneous transluminal coronary angioplasty catheter?

The FDA product code for Drug-eluting percutaneous transluminal coronary angioplasty catheter is OOB.

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Fuente oficial

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