阀门，肺
PMA编号：P180002 · 2026-09-11
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决定日期2026-09-11
PMA 编号P180002
产品代码NJK
设备分类第3类
医疗专科U
咨询委员会AN
请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。
器械摘要
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.
常见问题
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.
肺瓣膜的列名申请人是谁？
The FDA 510(k) record lists Pulmonx Corporation as the applicant. This does not by itself establish the device manufacturer.
肺瓣膜产品的FDA产品代码是什么？
FDA产品代码，肺瓣膜为NJK。
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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