K242206
- 510(k) number
- K242206
- Device name
- ACTIVO
- Applicant
- Daeju Meditech Engineering Co., Ltd. KR
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-09-27
- Date received
- 2024-07-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K242206.pdf
Official FDA record: K242206
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.