QZF
- 产品代码
- QZF
- 器械名称
- Gastrointestinal Capsule Endoscopy Analysis Software Device
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 876.1540
- FDA 专业组
- Gastroenterology, Urology
- 上市路径
- 需提交 510(k) 上市前通告
- 该代码近三年的 510(k)
- 2 件
- 其中 Summary 已存档
- 1 份,可直接下载
- FDA 历史累计 510(k)
- 2 件(全部年份;本站只收录近三年的明细)
FDA 分类定义
A gastrointestinal capsule endoscopy analysis software device is used to analyze pre-recorded capsule endoscopy videos of the gastrointestinal tract that are suspected of containing lesions. This device uses software algorithms to identify images and areas of interest as outputs to aid the clinician in analyzing suspected lesions, for clinician review of device outputs. The device may contain hardware to support interfacing with a capsule imaging system.
该代码近三年的 510(k)(2 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K250655 | 2026-03-12 | Digestaid - Artificial Intelligence De | Deep Capsule® (Deep Capsule US) | |
| DEN230027 | 2023-12-12 | Ankon Technologies Co., Ltd. | NaviCam ProScan | — |
FDA 官方分类页: QZF
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。