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Cryo-Thermo Compression Device (FGK002)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222136
510(k) Type
Traditional
Applicant
Suzhou MicroPort RehabTech (Group) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/8/2023
Days to Decision
232 days
Submission Type
Summary

Cryo-Thermo Compression Device (FGK002)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222136
510(k) Type
Traditional
Applicant
Suzhou MicroPort RehabTech (Group) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/8/2023
Days to Decision
232 days
Submission Type
Summary