K230500

Air Compression Therapy Recovery System (model: MF-AWI, MF-AWI.LED.A-801, MF-AWI.LED.B-801, MF-AWI.OLED.A-601, MF-AWI.LED.A-601, MF-AWI.LED.B-601, MF-AWI.OLED.A-401, MF-AWI.LED.A-401, MF-AWI.LED.B-401)

510(k) 号: K230500
器械名称: Air Compression Therapy Recovery System (model: MF-AWI, MF-AWI.LED.A-801, MF-AWI.LED.B-801, MF-AWI.OLED.A-601, MF-AWI.LED.A-601, MF-AWI.LED.B-601, MF-AWI.OLED.A-401, MF-AWI.LED.A-401, MF-AWI.LED.B-401)
申请人: Jiangsu Maxf Electric Appliance Co., Ltd. CN
产品代码: IRP — Massager, Powered Inflatable Tube
批准日期: 2023-10-26
受理日期: 2023-02-24
决定: Substantially Equivalent
审查途径: Traditional
咨询委员会: Physical Medicine

PDF下载 510(k) Summary本站存档 · 2.9 MB · FDA 公有领域文件

也可从 FDA 官方下载： K230500.pdf

FDA 官方记录： K230500

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。