K222400
- 510(k) number
- K222400
- Device name
- Coresculpt & Magsculpt
- Applicant
- K1Med Co., Ltd. KR
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2024-02-27
- Date received
- 2022-08-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
510(k) Summary (official FDA PDF): K222400.pdf
Official FDA record: K222400
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.