FDA 510(k)

Elecsys 地高辛免疫测定，Elecsys PreciControl 心脏 II

K号: K153301 · 2016-04-08

决定日期2016-04-08

产品代码KXT

咨询委员会TX 请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。

决定实质等同

器械摘要

Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics. It received FDA 510(k) clearance on 2016-04-08 under 510(k) number K153301. The device is classified under product code KXT. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II?

Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II is a medical device that received FDA 510(k) clearance on 2016-04-08. The listed applicant is Roche Diagnostics. The 510(k) number is K153301.

When did Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II receive FDA 510(k) clearance?

Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II received FDA 510(k) clearance on 2016-04-08, under 510(k) number K153301.

Who is the listed applicant for Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II?

FDA 510(k)记录显示罗氏诊断公司为申请人。这本身并不能确立该设备的制造商。

What is the FDA product code for Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II?

The FDA product code for Elecsys Digoxin Immunoassay, Elecsys PreciControl Cardiac II is KXT.

列明Roche Diagnostics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。

K261686Elecsys 磷酸-Tau（217P）血浆 K252323科博斯脉搏血糖监测系统 K252280Elecsys 抗-SARS-CoV-2 S K260049Elecsys Anti-HBc IgM K260046Elecsys Anti-HBc II K260048Elecsys Anti-HAV IgM

查看所有 69 个设备 →

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。