PIG
- 产品代码
- PIG
- 器械名称
- Acute Kidney Injury Test System
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 862.1220
- FDA 专业组
- Clinical Chemistry
- 上市路径
- 需提交 510(k) 上市前通告
- 该代码近三年的 510(k)
- 1 件
- 其中 Summary 已存档
- 1 份,可直接下载
- FDA 历史累计 510(k)
- 5 件(全部年份;本站只收录近三年的明细)
FDA 分类定义
An acute kidney injury test system is intended to measure one or more analytes in human samples as an aid in the assessment of a patient's risk for developing acute kidney injury. Test results are intended to be used in conjunction with other clinical and diagnostic findings, consistent with professional standards of practice, including conifmration by alternative methods.
该代码近三年的 510(k)(1 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K232761 | 2023-12-07 | Bioporto Diagnostic, Inc. | ProNephro AKI (NGAL) |
FDA 官方分类页: PIG
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。