PMA de la FDA

Pulmonary stent

Número de PMA: P220004 · 2024-09-05

SolicitanteCordis US Corp

Fecha de decisión2024-09-05

Número PMAP220004

Código de productoQWC

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorCV

Resumen del dispositivo

Pulmonary stent is the device name listed in this FDA 510(k) record. The listed applicant is Cordis US Corp. It received FDA 510(k) clearance on 2024-09-05. The device is classified under product code QWC. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Pulmonary stent?

Pulmonary stent is a medical device that received FDA 510(k) clearance on 2024-09-05. The listed applicant is Cordis US Corp.

When did Pulmonary stent receive FDA 510(k) clearance?

The clearance date for Pulmonary stent can be found in the official FDA records.

Who is the listed applicant for Pulmonary stent?

The FDA 510(k) record lists Cordis US Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pulmonary stent?

The FDA product code for Pulmonary stent is QWC.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.