LungQ 4
K号: K250766 · 2025-10-02
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器械摘要
LungQ 4 is the device name listed in this FDA 510(k) record. The listed applicant is Thirona BV. It received FDA 510(k) clearance on 2025-10-02 under 510(k) number K250766. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LungQ 4?
LungQ 4 is a medical device that received FDA 510(k) clearance on 2025-10-02. The listed applicant is Thirona BV. The 510(k) number is K250766.
When did LungQ 4 receive FDA 510(k) clearance?
LungQ 4 received FDA 510(k) clearance on 2025-10-02, under 510(k) number K250766.
Who is the listed applicant for LungQ 4?
The FDA 510(k) record lists Thirona BV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LungQ 4?
The FDA product code for LungQ 4 is JAK.
相关临床试验
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列明Thirona BV为申报人的其他记录
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相关器械（代码：JAK）
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。
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官方来源
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