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FDA 510(k)

AK 98 血液透析机,U9000 超滤器,C705 扩展室附件

K号: K201809 · 2021-03-10

决定日期2021-03-10
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

AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corportation. It received FDA 510(k) clearance on 2021-03-10 under 510(k) number K201809. 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 AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory?

AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory is a medical device that received FDA 510(k) clearance on 2021-03-10. The listed applicant is Baxter Healthcare Corportation. The 510(k) number is K201809.

When did AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory receive FDA 510(k) clearance?

AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory received FDA 510(k) clearance on 2021-03-10, under 510(k) number K201809.

Who is the listed applicant for AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory?

The FDA 510(k) record lists Baxter Healthcare Corportation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory?

The FDA product code for AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory 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Baxter Healthcare Corportation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。

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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