OLZ

Automatic Event Detection Software For Polysomnograph With Electroencephalograph

产品代码
OLZ
器械名称
Automatic Event Detection Software For 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
该代码近三年的 510(k)
37 件

FDA 分类定义

Automatically mark electroencephalograph and polysomongraph signals in order to aid in identification of such events and annotation of prolonged PSG traces; Automatically calculate simple measures obtained from recorded signals (e.G. Magnitude, time, frequency and simple statistical measures of marked events); All output subject to verification by qualified user

定义原文来自 FDA 器械分类库,属美国联邦政府作品(公有领域)。

该代码近三年的 510(k)(8 件)

数据窗口为最近三年。最新一件:2026-06-27。

510(k) 号批准日期申请人器械名称摘要
K2533902026-06-27Honeynaps Co., Ltd.SOMNUM (SOMNUM)PDF
K2536682026-03-08Onera B.V.Onera SleepMap (SLEEPMAP)FDA
K2508512025-12-14Cadwell Industries, Inc.Hypnos (369054-200)PDF
K2523302025-11-17Nox Medical EhfDeepRESPPDF
K2500582025-04-10Brain Electrophysiology Laboratory ComNEAT 001PDF
K2419602025-03-14Nox Medical EhfDeepRESPPDF
K2420942024-11-22Beacon Biosignals, Inc.Dreem 3SPDF
K2334382024-03-08Beacon Biosignals, Inc.SleepStageMLPDF

其中 7 件的 Summary 已存档在本站,点 PDF 直接下载;其余给 FDA 官方链接。

FDA 官方分类页: OLZ
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。