K241157
- 510(k) number
- K241157
- Device name
- Secret MAX Multi-platform RF System
- Applicant
- Ilooda Co,., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-11-21
- Date received
- 2024-04-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K241157
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.