K244059

HydroMID 5F Dual Lumen Midline Catheter - Basic Kit (70006102); HydroMID 5F Dual Lumen Midline Catheter - Max Barrier Kit (70006104); HydroMID 5F Dual Lumen Midline Catheter - Mobile Max Barrier Kit (90006104)

510(k) 号: K244059
器械名称: HydroMID 5F Dual Lumen Midline Catheter - Basic Kit (70006102); HydroMID 5F Dual Lumen Midline Catheter - Max Barrier Kit (70006104); HydroMID 5F Dual Lumen Midline Catheter - Mobile Max Barrier Kit (90006104)
申请人: Access Vascular, Inc. MD · US
产品代码: FOZ — Catheter, Intravascular, Therapeutic, Short-Term Les
批准日期: 2025-03-27
受理日期: 2024-12-31
决定: Substantially Equivalent
审查途径: Special
咨询委员会: General Hospital

PDF下载 510(k) Summary本站存档 · 2.5 MB · FDA 公有领域文件

也可从 FDA 官方下载： K244059.pdf

FDA 官方记录： K244059

数据来自 openFDA 510(k) 数据集（CC0 公有领域），以 FDA 现行记录为准。510(k) 许可不等于 FDA 认证或批准。