meddevicedb.com FDA Device Reference

EXCELART VANTAGE ZGV

K060003 Class II Traditional
Decision Date
2006-01-18
Sponsor / Applicant
Toshibamedical Systems Corporation

Technical Specification

510(k) Submission ID K060003
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2006-01-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXCELART VANTAGE ZGV received FDA 510(k) clearance under submission number K060003, sponsored by Toshibamedical Systems Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-01-18.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.