Last synced on 25 January 2026 at 3:41 am

Coresculpt & Magsculpt

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222400
510(k) Type
Traditional
Applicant
K1Med Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/27/2024
Days to Decision
567 days
Submission Type
Summary

Coresculpt & Magsculpt

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222400
510(k) Type
Traditional
Applicant
K1Med Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/27/2024
Days to Decision
567 days
Submission Type
Summary