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FDA 510(k)

FX CorAL 40;FX CorAL 50

K号: K253518 · 2025-12-18

决定日期2025-12-18
产品代码KDI
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

FX CorAL 40; FX CorAL 50 is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius Medical Care Renal Therapies Group, LLC. It received FDA 510(k) clearance on 2025-12-18 under 510(k) number K253518. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FX CorAL 40; FX CorAL 50?

FX CorAL 40; FX CorAL 50 is a medical device that received FDA 510(k) clearance on 2025-12-18. The listed applicant is Fresenius Medical Care Renal Therapies Group, LLC. The 510(k) number is K253518.

When did FX CorAL 40; FX CorAL 50 receive FDA 510(k) clearance?

FX CorAL 40; FX CorAL 50 received FDA 510(k) clearance on 2025-12-18, under 510(k) number K253518.

Who is the listed applicant for FX CorAL 40; FX CorAL 50?

FDA 510(k)记录中列出Fresenius Medical Care Renal Therapies Group, LLC为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for FX CorAL 40; FX CorAL 50?

The FDA product code for FX CorAL 40; FX CorAL 50 is KDI.

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。

列明Fresenius Medical Care Renal Therapies Group, LLC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。

查看所有 48 个设备 →

相关器械(代码:KDI)

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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