K233374
- 510(k) number
- K233374
- Device name
- Secret Pro
- Applicant
- Ilooda Co,., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2023-12-14
- Date received
- 2023-10-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- 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: K233374
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.