QWT

Prognostic Assessment Software Of Mild Cognitive Impairment

产品代码
QWT
器械名称
Prognostic Assessment Software Of Mild Cognitive Impairment
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 882.1454
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)
1 件
其中 Summary 已存档
0 份,可直接下载
FDA 历史累计 510(k)
1 件(全部年份;本站只收录近三年的明细)

FDA 分类定义

Prognostic assessment software of mild cognitive impairment. Prognostic assessment software of mild cognitive impairment is a prescription-only device that combines information from multiple clinical data sources to produce an output indicative of the likelihood that a patient diagnosed with mild cognitive impairment will progress to more severe forms of cognitive impairment, or will develop dementia, such as Alzheimer’s disease dementia, within a specified period of time. This device is intended for adjunctive use and not intended as a stand-alone diagnostic or prognostic too.

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)(1 件)

数据窗口为最近三年。最新一件:2024-01-11。

510(k) 号批准日期申请人器械名称摘要
DEN2200662024-01-11Darmiyan, Inc.BrainSee
FDA 官方分类页: QWT
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。