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Jiangsu Maxf Electric Appliance Co., Ltd.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) 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)IRP2023-10-26 View
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