LungQ软件
K号: K173821 · 2018-06-05
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器械摘要
LungQ Software is the device name listed in this FDA 510(k) record. The listed applicant is Thirona Corporation. It received FDA 510(k) clearance on 2018-06-05 under 510(k) number K173821. 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 Software?
LungQ Software is a medical device that received FDA 510(k) clearance on 2018-06-05. The listed applicant is Thirona Corporation. The 510(k) number is K173821.
When did LungQ Software receive FDA 510(k) clearance?
LungQ Software received FDA 510(k) clearance on 2018-06-05, under 510(k) number K173821.
Who is the listed applicant for LungQ Software?
The FDA 510(k) record lists Thirona Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LungQ Software?
The FDA product code for LungQ Software is JAK.
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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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