OZE

Influenza A And Influenza B Multiplex Nucleic Acid Assay

产品代码
OZE
器械名称
Influenza A And Influenza B Multiplex Nucleic Acid Assay
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 866.3980
FDA 专业组
Microbiology
上市路径
需提交 510(k) 上市前通告
该代码近三年的 510(k)
3 件
其中 Summary 已存档
3 份,可直接下载
FDA 历史累计 510(k)
20 件(全部年份;本站只收录近三年的明细)

FDA 分类定义

An Influenza A and Influenza B multiplex nucleic acid assay is a multiplex in vitro diagnostic test for the simultaneous qualitative detection and discrimination of influenza A and influenza B nucleic acids isolated and purified from human respiratory specimens obtained from individuals exhibiting signs and symptoms of respiratory tract infections or viral culture. The detection and discrimination of influenza A and B nucleic acids from symptomatic patients aid in the diagnosis of human respiratory tract influenza viral infections if used in conjunction with other clinical and laboratory findings.

定义原文来自 FDA 器械分类库,属美国联邦政府作品(公有领域)。

该代码近三年的 510(k)(3 件)

数据窗口为最近三年。最新一件:2025-07-11。

510(k) 号批准日期申请人器械名称摘要
K2432742025-07-11Centers for Disease Control and Preven…CDC Human Influenza Virus Real-Time RT-PCR Diagnosti…PDF
K2439312025-03-14Centers for Disease Control and Preven…CDC Human Influenza Virus Real-time RT-PCR Diagnosti…PDF
K2411102024-05-21Centers for Disease Control and Preven…CDC Human Influenza Virus Real-Time RT-PCR Diagnosti…PDF

其中 3 件的 Summary 已存档在本站,点 PDF 直接下载;其余给 FDA 官方链接。

FDA 官方分类页: OZE
分类与上市路径以 FDA 现行公告为准。本页数据来自 openFDA(CC0 公有领域),不构成注册策略建议。