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Coresculpt & Magsculpt

Page Type
Cleared 510(K)
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)
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