OZE
- 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.
该代码近三年的 510(k)(3 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K243274 | 2025-07-11 | Centers for Disease Control and Preven… | CDC Human Influenza Virus Real-Time RT-PCR Diagnosti… | |
| K243931 | 2025-03-14 | Centers for Disease Control and Preven… | CDC Human Influenza Virus Real-time RT-PCR Diagnosti… | |
| K241110 | 2024-05-21 | Centers for Disease Control and Preven… | CDC Human Influenza Virus Real-Time RT-PCR Diagnosti… |
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。