K260972
- 510(k) number
- K260972
- Device name
- OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD Monitor
- Applicant
- Sony Corporation JP
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2026-08-26
- Date received
- 2026-03-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
510(k) Summary (official FDA PDF): K260972.pdf
Official FDA record: K260972
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.