K252985
- 510(k) number
- K252985
- Device name
- Laport
- Applicant
- Sejong Medical Co., Ltd. KR
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2026-05-19
- Date received
- 2025-09-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
510(k) Summary (official FDA PDF): K252985.pdf
Official FDA record: K252985
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.