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Leg and Foot Air Wave Pressure Therapy Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223464
510(k) Type
Traditional
Applicant
Zhangzhou Easepal Innovation CO , Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/14/2023
Days to Decision
117 days
Submission Type
Summary

Leg and Foot Air Wave Pressure Therapy Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223464
510(k) Type
Traditional
Applicant
Zhangzhou Easepal Innovation CO , Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/14/2023
Days to Decision
117 days
Submission Type
Summary