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FDA 510(k)

AMICUS 分离系统，AMICUS 交换包 - 治疗品，废物转移套装，带排气针和卢瑞适配器的血液成分过滤器套装

K号: K180615 · 2018-12-04

申请人Fresenius Kabi USA,Llc
决定日期2018-12-04
产品代码LKN
决定实质等同

器械摘要

AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius Kabi USA,Llc. It received FDA 510(k) clearance on 2018-12-04 under 510(k) number K180615. The device is classified under product code LKN. FDA Decision: Substantially Equivalent.

常见问题

What is the AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter?

AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter is a medical device that received FDA 510(k) clearance on 2018-12-04. The listed applicant is Fresenius Kabi USA,Llc. The 510(k) number is K180615.

When did AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter receive FDA 510(k) clearance?

AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter received FDA 510(k) clearance on 2018-12-04, under 510(k) number K180615.

Who is the listed applicant for AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter?

The FDA 510(k) record lists Fresenius Kabi USA,Llc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter?

The FDA product code for AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter is LKN.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Fresenius Kabi USA,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。

K162462AMICUS 分离系统，AMICUS 分离系统；翻新

相关器械（代码：LKN）

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。

K192150AMICUS 分离系统Fresenius Kabi AGK183081Spectra Optia 血浆分离系统Terumobct, Inc.K181049Spectra Optia 血浆分离系统Terumobct, Inc.K172590Spectra Optia 血浆分离系统Terumobct, Inc.K153601Spectra Optia 血浆分离系统Terumobct, Inc.

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

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