Last synced on 25 January 2026 at 3:41 am

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)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230500
510(k) Type
Traditional
Applicant
Jiangsu Maxf Electric Appliance Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/26/2023
Days to Decision
244 days
Submission Type
Summary

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)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230500
510(k) Type
Traditional
Applicant
Jiangsu Maxf Electric Appliance Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/26/2023
Days to Decision
244 days
Submission Type
Summary