LIT

Catheter, Angioplasty, Peripheral, Transluminal

产品代码
LIT
器械名称
Catheter, Angioplasty, Peripheral, Transluminal
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
标记
可走第三方审查
该代码近三年的 510(k)
403 件

该代码近三年的 510(k)(12 件)

数据窗口为最近三年。最新一件:2026-05-20。

510(k) 号批准日期申请人器械名称
K2603042026-05-20WAVE Medical AGWAVE PTA Balloon Catheter 摘要
K2525122026-02-13ABBOTT MEDICALArmada™ 14 NC PTA Catheter 摘要
K2519152025-12-18Natec Medical , Ltd.Amethyst HP PTA OTW 0.035 Catheter 摘要
K2507062025-04-04Biotronik, Inc.Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo 摘要
K2437042025-02-27Brosmed Medical Co., Ltd.Parafleet SC 014 PTA Balloon Dilatation Catheter; Pa 摘要
K2410402024-12-18Natec Medical , Ltd.Amethyst HP PTA OTW 0.035 Catheter 摘要
K2424192024-11-15Creagh Medical Ltd. Dba Surmodics, Inc018 Hydrophilic Coated OTW PTA Balloon Dilatation Ca 摘要
K2417402024-07-16Summa TherapeuticsFinesse Injectable™ PTA Balloon Dilatation Catheter 摘要
K2417112024-07-11Biotronik, Inc.Oscar Peripheral Multifunctional Catheter system 摘要
K2416832024-07-10Boston Scientific CorporationSterling™ MONORAIL™ PTA Balloon Dilatation Catheter 摘要
K2410252024-06-11OrbusNeich Medical (Shenzhen) Co., LtdJADE PLUS PTA Balloon Dilatation Catheter 摘要
K2314022023-12-20Kossel Medtech (Suzhou) Co., Ltd.HP PTA Balloon Dilatation Catheter 摘要
FDA 官方分类页: LIT
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。