QQX

Respiratory Specimen Nucleic Acid Sars-Cov-2 Test

产品代码
QQX
器械名称
Respiratory Specimen Nucleic Acid Sars-Cov-2 Test
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 866.3981
FDA 专业组
Microbiology
上市路径
需提交 510(k) 上市前通告
该代码近三年的 510(k)
6 件
其中 Summary 已存档
6 份,可直接下载
FDA 历史累计 510(k)
11 件(全部年份;本站只收录近三年的明细)

FDA 分类定义

A device to detect and identify nucleic acid targets in respiratory specimens from SARS-CoV-2 that cause COVID-19 is an in vitro diagnostic device intended for the detection and identification of SARS-CoV-2 nucleic acid targets in human clinical respiratory specimens from patients suspected of COVID-19 based on signs and symptoms of respiratory infections by their healthcare providers. The device is intended to aid in the diagnosis of COVID-19 in conjunction with other clinical, epidemiologic, and laboratory data or other risk factors.

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)(6 件)

数据窗口为最近三年。最新一件:2025-02-13。

510(k) 号批准日期申请人器械名称摘要
K2433962025-02-13Hologic, Inc.Aptima SARS-CoV-2 AssayPDF
K2408672025-02-11Roche Molecular Systems, Inc.cobas® SARS-CoV-2 Qualitative for use on the cobas® …PDF
K2421092025-01-15Cepheid®Xpert® Xpress CoV-2 plus (XPRS-COV2-10)PDF
K2415802024-12-06Abbott MolecularAlinity m SARS-CoV-2 AMP Kit (09N78-096); Alinity m …PDF
K2334532024-07-10Life Technologies CorporationApplied Biosystems™ TaqPath™ COVID-19 Diagnostic PC…PDF
K2304402023-10-13Cepheid®Xpert® Xpress CoV-2 plusPDF

其中 6 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: QQX
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。