FDA PMA

Pulmonary stent

Número do PMA: P220004 · 2024-09-05

RequerenteCordis US Corp

Data da decisão2024-09-05

Número PMAP220004

Código do produtoQWC

Classe do DispositivoClasse 3

Especialidade MédicaU

Comité consultivoCV

Resumo do 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.

Perguntas frequentes

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.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

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

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.