FDA PMA

Stent, central venous

Número do PMA: P980033 · 2026-05-06

RequerenteBoston Scientific Corporation

Data da decisão2026-05-06

Número PMAP980033

Código do produtoQKJ

Classe do DispositivoClasse 3

Especialidade MédicaU

Comité consultivoCV

Resumo do dispositivo

Stent, central venous is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2026-05-06. The device is classified under product code QKJ. It was reviewed by the CV advisory panel.

Perguntas frequentes

What is the Stent, central venous?

Stent, central venous is a medical device that received FDA 510(k) clearance on 2026-05-06. The listed applicant is Boston Scientific Corporation.

When did Stent, central venous receive FDA 510(k) clearance?

The clearance date for Stent, central venous can be found in the official FDA records.

Who is the listed applicant for Stent, central venous?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stent, central venous?

The FDA product code for Stent, central venous is QKJ.

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Fonte oficial

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