meddevicedb.com FDA Device Reference

cvi42 Coronary Plaque Software Application

K251027 Class II Traditional
Decision Date
2025-10-27
Sponsor / Applicant
Circle Cardiovascular Imaging, Inc.

Technical Specification

510(k) Submission ID K251027
Product Code QIH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2025-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

cvi42 Coronary Plaque Software Application received FDA 510(k) clearance under submission number K251027, sponsored by Circle Cardiovascular Imaging, 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 2025-10-27.

Classification & Regulation

This clearance is catalogued under FDA product code QIH and 21 CFR 892.2050, within the Radiology review panel as a Class II device.