meddevicedb.com FDA Device Reference

CT EXPRES III CONTRAST MEDIA DELIVERY SYSTEM

K062265 Class II Traditional
Decision Date
2006-12-26
Sponsor / Applicant
Swiss Medical Care S.A.

Technical Specification

510(k) Submission ID K062265
Product Code IZQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 2006-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CT EXPRES III CONTRAST MEDIA DELIVERY SYSTEM received FDA 510(k) clearance under submission number K062265, sponsored by Swiss Medical Care S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-12-26.

Classification & Regulation

This clearance is catalogued under FDA product code IZQ and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.