FDA 510(k)

LVivo无缝

K号: K243331 · 2025-03-06

决定日期2025-03-06

产品代码QIH

咨询委员会RA

决定实质等同

器械摘要

LVivo Seamless is the device name listed in this FDA 510(k) record. The listed applicant is Dia Imaging Analysis, Ltd.. It received FDA 510(k) clearance on 2025-03-06 under 510(k) number K243331. 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 LVivo Seamless?

LVivo Seamless is a medical device that received FDA 510(k) clearance on 2025-03-06. The listed applicant is Dia Imaging Analysis, Ltd.. The 510(k) number is K243331.

When did LVivo Seamless receive FDA 510(k) clearance?

LVivo Seamless received FDA 510(k) clearance on 2025-03-06, under 510(k) number K243331.

Who is the listed applicant for LVivo Seamless?

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

What is the FDA product code for LVivo Seamless?

The FDA product code for LVivo Seamless is QIH.

列明Dia Imaging Analysis, 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。

K243862LVivo软件应用 K243235LVivo软件应用 K240553LVivo软件应用 K240769LVivo IQS K222970LVivo IQS K212466LVivo无缝

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