meddevicedb.com FDA Device Reference

Vitrea CT VScore

K243240 Class II Traditional
Decision Date
2025-04-10
Sponsor / Applicant
Canon Medical Informatics, Inc.

Technical Specification

510(k) Submission ID K243240
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2025-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Vitrea CT VScore received FDA 510(k) clearance under submission number K243240, sponsored by Canon Medical Informatics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.