FDA PMA

Valve, pulmonary

Número do PMA: P180002 · 2026-09-11

RequerentePulmonx Corporation

Data da decisão2026-09-11

Número PMAP180002

Código do produtoNJK

Classe do DispositivoClasse 3

Especialidade MédicaU

Comité consultivoAN

Resumo do dispositivo

Valve, pulmonary is the device name listed in this FDA 510(k) record. The listed applicant is Pulmonx Corporation. It received FDA 510(k) clearance on 2026-09-11. The device is classified under product code NJK. It was reviewed by the AN advisory panel.

Perguntas frequentes

What is the Valve, pulmonary?

Valve, pulmonary is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Pulmonx Corporation.

When did Valve, pulmonary receive FDA 510(k) clearance?

The clearance date for Valve, pulmonary can be found in the official FDA records.

Who is the listed applicant for Valve, pulmonary?

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

What is the FDA product code for Valve, pulmonary?

The FDA product code for Valve, pulmonary is NJK.

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Fonte oficial

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