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Air Compression Therapy Device, model: ST-502

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213745
510(k) Type
Traditional
Applicant
Shenzhen Future Electronic Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/31/2022
Days to Decision
122 days
Submission Type
Summary

Air Compression Therapy Device, model: ST-502

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213745
510(k) Type
Traditional
Applicant
Shenzhen Future Electronic Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/31/2022
Days to Decision
122 days
Submission Type
Summary