meddevicedb.com FDA Device Reference

AQUILION SUPER 4 MULTISLICE CT SCANNER, MODEL TSX-101A/7

K031469 Class II Traditional
Decision Date
2003-05-22
Sponsor / Applicant
Toshiba America Medical Systems, In.C

Technical Specification

510(k) Submission ID K031469
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2003-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AQUILION SUPER 4 MULTISLICE CT SCANNER, MODEL TSX-101A/7 received FDA 510(k) clearance under submission number K031469, sponsored by Toshiba America Medical Systems, In.C. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-05-22.

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.