PCH
- 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.
该代码近三年的 510(k)(13 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K253722 | 2026-05-19 | Luminex Corporation | LIAISON PLEX Gastrointestinal Flex Assay | |
| K254032 | 2026-03-09 | QIAGEN GmbH | QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI P… | |
| K251721 | 2026-01-16 | Cepheid | Xpert GI Panel | |
| K252329 | 2025-10-22 | QIAGEN GmbH | QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI P… | |
| K251868 | 2025-09-25 | Hologic | Panther Fusion GI Bacterial Assay | |
| K251993 | 2025-09-25 | Hologic, Inc. | Panther Fusion GI Expanded Bacterial Assay | |
| K250324 | 2025-02-28 | QIAGEN GmbH | QIAstat-Dx GI Panel 2 Mini B | |
| K243885 | 2025-01-16 | Biofire Diagnostics, LLC | BIOFIRE FILMARRAY Gastrointestinal (GI) Panel Mid | |
| K242877 | 2025-01-10 | Applied BioCode, Inc. | BioCode Gastrointestinal Pathogen Panel (GPP) | |
| K243813 | 2025-01-08 | QIAGEN GmbH | QIAstat-Dx GI Panel 2 Mini B&V | |
| K242367 | 2024-11-07 | Biofire Diagnostics, LLC | BIOFIRE FILMARRAY Gastrointestinal (GI) Panel | |
| K220062 | 2024-05-31 | QIAGEN GmbH | QIAstat-Dx Gastrointestinal Panel 2 | |
| K232672 | 2024-05-29 | Genetic Signatures Limited | EasyScreen Gastrointestinal Parasite Detection Kit |
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。