FDA
- 产品代码
- FDA
- 器械名称
- Enteroscope And Accessories
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 876.1500
- 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)
- 20 件
FDA 分类定义
To provide visualization and perform various procedures within the small intestine. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
该代码近三年的 510(k)(3 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K260314 | 2026-05-01 | Aspero Medical, Inc. | Ancora-SB | |
| K251204 | 2025-09-26 | FUJIFILM Healthcare Americas Corporati | FUJIFILM Stiffening Wire Device (SW-2000) | FDA |
| K233321 | 2024-06-13 | FUJIFILM Healthcare Americas Corporati | Double Balloon Endoscope EN-840T, Over-tube TS-1214 |
FDA 官方分类页: FDA
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。