FDA 510(k) Applications Submitted by Jiangsu MaxF Electric Appliance Co., Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K230500 02/24/2023 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) Jiangsu MaxF Electric Appliance Co., Ltd


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact