SEM
- 产品代码
- SEM
- 器械名称
- Sub-Scalp Implanted Electroencephalogram System For Remote Patient Monitoring
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 882.1360
- FDA 专业组
- Neurology
- 上市路径
- 需提交 510(k) 上市前通告
- 标记
- 属植入器械
- 该代码近三年的 510(k)
- 2 件
- 其中 Summary 已存档
- 1 份,可直接下载
- FDA 历史累计 510(k)
- 2 件(全部年份;本站只收录近三年的明细)
FDA 分类定义
A sub-scalp implanted electroencephalogram (EEG) system for remote patient monitoring is a prescription device used for continuously acquiring, transmitting, and storing electrical brain activity of patients with epilepsy. The device consists of sub-scalp implanted electrodes that are connected to a transmitter or storage device. The device is used to aid clinicians in the remote monitoring of electrical activity in the patients brain. The device is not intended to be implanted in brain tissue.
该代码近三年的 510(k)(2 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K253607 | 2026-06-11 | Uneeg Medical A/S | UNEEG EpiSight System | |
| DEN240062 | 2025-04-17 | Epi-Minder Pty, Ltd. | Minder System | — |
FDA 官方分类页: SEM
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。