K242907
- 510(k) number
- K242907
- Device name
- DELPHI System
- Applicant
- CnS Medical Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-06-06
- Date received
- 2024-09-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K242907.pdf
Official FDA record: K242907
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.