meddevicedb.com FDA Device Reference

QANGIO CT

K062386 Class II Traditional
Decision Date
2006-10-05
Sponsor / Applicant
Medis Medical Imaging Systems BV

Technical Specification

510(k) Submission ID K062386
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2006-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QANGIO CT received FDA 510(k) clearance under submission number K062386, sponsored by Medis Medical Imaging Systems BV. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-10-05.

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.