MCW

Catheter, Peripheral, Atherectomy

产品代码
MCW
器械名称
Catheter, Peripheral, Atherectomy
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 870.4875
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)
146 件

该代码近三年的 510(k)(9 件)

数据窗口为最近三年。最新一件:2026-04-10。

510(k) 号批准日期申请人器械名称
K2602442026-04-10Eximo MedicalAuryon Atherectomy System 摘要
K2507232025-04-25Cardio Flow Inc.,FreedomFlow™ Orbital Circumferential Atherectomy Sys 摘要
K2503852025-03-13SpectraneticsTurbo-Elite Laser Atherectomy Catheter 摘要
K2427572025-01-30Bard Peripheral Vascular, Inc.Rotarex Atherectomy System 摘要
K2429472024-11-05Cardio Flow Inc.,FreedomFlow™ Orbital Circumferential Atherectomy Sys 摘要
K2415532024-06-27Eximo Medical, Ltd.Auryon Atherectomy Catheter 1.7mm; Auryon Atherectom 摘要
K2334832024-02-15Cardio Flow Inc.,FreedomFlow Orbital Circumferential Atherectomy Syst 摘要
K2336682023-12-15Eximo Medical, Ltd.Auryon Atherectomy Catheter 1.5 mm XL, Hydrophilic C 摘要
K2315382023-09-27Cardio Flow Inc.,FreedomFlow Orbital Circumferential Atherectomy Syst 摘要
FDA 官方分类页: MCW
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。