PCH

Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System

产品代码
PCH
器械名称
Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 866.3990
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)
13 件
其中 Summary 已存档
13 份,可直接下载
FDA 历史累计 510(k)
38 件(全部年份;本站只收录近三年的明细)

FDA 分类定义

A gastrointestinal pathogen panel multiplex nucleic acid assay is a qualitative in vitro diagnostic device intended to simultaneously detect and identify multiple gastrointestinal microbial nucleic acids extracted from human stool specimens. The detection and identification of a specific gastrointestinal microbial nucleic acid from individuals exhibiting signs and/or symptoms of gastrointestinal infection aids in the diagnosis of gastrointestinal infection when used in conjunction with clinical evaluation and other laboratory findings.

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)(13 件)

数据窗口为最近三年。最新一件:2026-05-19。

510(k) 号批准日期申请人器械名称摘要
K2537222026-05-19Luminex CorporationLIAISON PLEX Gastrointestinal Flex AssayPDF
K2540322026-03-09QIAGEN GmbHQIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI P…PDF
K2517212026-01-16CepheidXpert GI PanelPDF
K2523292025-10-22QIAGEN GmbHQIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI P…PDF
K2518682025-09-25HologicPanther Fusion GI Bacterial AssayPDF
K2519932025-09-25Hologic, Inc.Panther Fusion GI Expanded Bacterial AssayPDF
K2503242025-02-28QIAGEN GmbHQIAstat-Dx GI Panel 2 Mini BPDF
K2438852025-01-16Biofire Diagnostics, LLCBIOFIRE FILMARRAY Gastrointestinal (GI) Panel MidPDF
K2428772025-01-10Applied BioCode, Inc.BioCode Gastrointestinal Pathogen Panel (GPP)PDF
K2438132025-01-08QIAGEN GmbHQIAstat-Dx GI Panel 2 Mini B&VPDF
K2423672024-11-07Biofire Diagnostics, LLCBIOFIRE FILMARRAY Gastrointestinal (GI) PanelPDF
K2200622024-05-31QIAGEN GmbHQIAstat-Dx Gastrointestinal Panel 2PDF
K2326722024-05-29Genetic Signatures LimitedEasyScreen Gastrointestinal Parasite Detection KitPDF

其中 13 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: PCH
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。