FDA 510(k)

LungVision

K号: K240943 · 2024-10-01

决定日期2024-10-01

产品代码QIH

咨询委员会RA

决定实质等同

器械摘要

LungVision is the device name listed in this FDA 510(k) record. The listed applicant is Bodyvision Medical , Ltd.. It received FDA 510(k) clearance on 2024-10-01 under 510(k) number K240943. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LungVision?

LungVision is a medical device that received FDA 510(k) clearance on 2024-10-01. The listed applicant is Bodyvision Medical , Ltd.. The 510(k) number is K240943.

When did LungVision receive FDA 510(k) clearance?

LungVision received FDA 510(k) clearance on 2024-10-01, under 510(k) number K240943.

Who is the listed applicant for LungVision?

The FDA 510(k) record lists Bodyvision Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LungVision?

The FDA product code for LungVision is QIH.

列明Bodyvision Medical , Ltd.为申报人的其他记录

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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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。