PDU
- 产品代码
- PDU
- 器械名称
- Catheter For Crossing Total Occlusions
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 870.1250
- FDA 专业组
- Cardiovascular
- 上市路径
- 需提交 510(k) 上市前通告
- 该代码近三年的 510(k)
- 58 件
FDA 分类定义
To facilitate the intraluminal placement of conventional guidewires beyond stenotic lesions (including subchronic and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention, such as angioplasty, atherectomy or stent placement.
该代码近三年的 510(k)(5 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K262013 | 2026-08-28 | Reflow Medical, Inc. | Kiba CTO Crossing Catheter | |
| K252315 | 2025-09-22 | AngioSafe, Inc. | Santreva-ATK Endovascular Revasculariztion Catheter | |
| K251158 | 2025-09-11 | Baylis Medical Technologies, Inc. | PowerWire® 14 Radiofrequency Guidewire Kit | |
| K251376 | 2025-05-31 | LimFlow, Inc. | LimFlow ARC | |
| K232562 | 2024-02-28 | Baylis Medical Technologies, Inc. | PowerWire Radiofrequency Guidewire Kit |
FDA 官方分类页: PDU
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。