meddevicedb.com FDA Device Reference

cvi42 Auto Imaging Software Application

K213998 Class II Traditional
Decision Date
2022-07-28
Sponsor / Applicant
Circle Cardiovascular Imaging, Inc.

Technical Specification

510(k) Submission ID K213998
Product Code QIH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2022-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

cvi42 Auto Imaging Software Application received FDA 510(k) clearance under submission number K213998, 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 2022-07-28.

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.