SEI
- 产品代码
- SEI
- 器械名称
- Qualitative And Quantitative Hepatitis B Virus Antibody Assays
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 866.3173
- 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)
- 4 件
- 其中 Summary 已存档
- 4 份,可直接下载
- FDA 历史累计 510(k)
- 4 件(全部年份;本站只收录近三年的明细)
FDA 分类定义
In vitro diagnostic devices intended for use in the detection of antibodies to HBV. These devices are intended to aid in the diagnosis of HBV infection in persons with signs and symptoms of hepatitis and in persons at risk for HBV infection. Anti-HBs assay results may be used as an aid in the determination of susceptibility to HBV infection in individuals prior to or following HBV vaccination or when vaccination status is unknown.
该代码近三年的 510(k)(4 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K260046 | 2026-04-07 | Roche Diagnostics | Elecsys Anti-HBc II | |
| K260049 | 2026-04-07 | Roche Diagnostics | Elecsys Anti-HBc IgM | |
| K254059 | 2026-03-13 | Beckman Coulter, Inc. | Access anti-HBc IgM | |
| K253687 | 2026-02-19 | Beckman Coulter, Inc. | Access anti-HBc Total |
FDA 官方分类页: SEI
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。