OLV
- 产品代码
- OLV
- 器械名称
- Standard Polysomnograph With Electroencephalograph
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 882.1400
- FDA 专业组
- Neurology
- 上市路径
- 需提交 510(k) 上市前通告
- 标记
- 可走第三方审查
- 该代码近三年的 510(k)
- 65 件
FDA 分类定义
Acquire, display, store, and archive electroencephalographic signals from the brain and other signals (such as electromyography, respiratory and/or oximetry signals) for sleep recordings. May also be used to allow on-screen review, user-controlled annotation and user-controlled marking of data.
该代码近三年的 510(k)(5 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K261747 | 2026-08-25 | Beacon Biosignals, Inc. | Report Studio | |
| K260585 | 2026-03-20 | Nox Medical Ehf | Noxturnal Web | |
| K242447 | 2025-02-20 | Compumedics Limited | Falcon HST | FDA |
| K241288 | 2024-12-23 | Nox Medical Ehf | Noxturnal Web | FDA |
| K240700 | 2024-12-08 | Somnomedics GmbH | HomeSleepTest (HST, HST REM+) |
FDA 官方分类页: OLV
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。