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FDA 510(k)

Optilite® Freelite® Kappa Free Kit,Optilite® Freelite® Lambda Free Kit

K号: K231290 · 2024-01-24

决定日期2024-01-24
产品代码DFH
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决定实质等同

器械摘要

Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit is the device name listed in this FDA 510(k) record. The listed applicant is The Binding Site, Ltd.. It received FDA 510(k) clearance on 2024-01-24 under 510(k) number K231290. The device is classified under product code DFH. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit?

Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit is a medical device that received FDA 510(k) clearance on 2024-01-24. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K231290.

When did Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit receive FDA 510(k) clearance?

Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit received FDA 510(k) clearance on 2024-01-24, under 510(k) number K231290.

Who is the listed applicant for Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit?

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

What is the FDA product code for Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit?

The FDA product code for Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit is DFH.

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。

相关器械(代码:DFH)

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

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