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FDA 510(k)

SC+ 血液透析设备,SC+ 透析液胶囊,SC+ 血管套管套装

K号: K222067 · 2022-11-10

决定日期2022-11-10
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

SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set is the device name listed in this FDA 510(k) record. The listed applicant is Quanta Dialysis Technologies, Ltd.. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K222067. 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 SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set?

SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Quanta Dialysis Technologies, Ltd.. The 510(k) number is K222067.

When did SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set receive FDA 510(k) clearance?

SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set received FDA 510(k) clearance on 2022-11-10, under 510(k) number K222067.

Who is the listed applicant for SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set?

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

What is the FDA product code for SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set?

The FDA product code for SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube Set 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Quanta Dialysis Technologies, 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。

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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