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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

Coresculpt & Magsculpt

Manufacturer

K1MED Co., Ltd.

Date Cleared

2024-02-27

(567 days)

Product Code

Regulation Number

Type

Panel

Physical Medicine

Age Range

N/A

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N/A

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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