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FDA 510(k)

DCX 一次性盒式(DCX)

K号: K243998 · 2025-04-25

决定日期2025-04-25
产品代码KDN
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定实质等同

器械摘要

DCX Disposable Cassette (DCX) is the device name listed in this FDA 510(k) record. The listed applicant is Institut Geroges Lopez. It received FDA 510(k) clearance on 2025-04-25 under 510(k) number K243998. The device is classified under product code KDN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the DCX Disposable Cassette (DCX)?

DCX Disposable Cassette (DCX) is a medical device that received FDA 510(k) clearance on 2025-04-25. The listed applicant is Institut Geroges Lopez. The 510(k) number is K243998.

When did DCX Disposable Cassette (DCX) receive FDA 510(k) clearance?

DCX Disposable Cassette (DCX) received FDA 510(k) clearance on 2025-04-25, under 510(k) number K243998.

Who is the listed applicant for DCX Disposable Cassette (DCX)?

The FDA 510(k) record lists Institut Geroges Lopez as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DCX Disposable Cassette (DCX)?

The FDA product code for DCX Disposable Cassette (DCX) is KDN.

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:KDN)

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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