meddevicedb.com FDA Device Reference

ImagenUniversal

K173547 Class II Traditional
Decision Date
2018-01-12
Sponsor / Applicant
Cardiovascular Imaging Technologies

Technical Specification

510(k) Submission ID K173547
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2018-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ImagenUniversal received FDA 510(k) clearance under submission number K173547, sponsored by Cardiovascular Imaging Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2018-01-12.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.