meddevicedb.com FDA Device Reference

ULTRAFAST CT SCANNER; EBT CT SCANNER, EVOLUTION

K972879 Class II Traditional
Decision Date
1997-10-15
Sponsor / Applicant
Imatron, Inc.

Technical Specification

510(k) Submission ID K972879
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1997-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRAFAST CT SCANNER; EBT CT SCANNER, EVOLUTION received FDA 510(k) clearance under submission number K972879, sponsored by Imatron, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-10-15.

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.