meddevicedb.com FDA Device Reference

SHIMAZU WHOLE BODY X-RAY CT SCANNER SCT-4800TF/GR

K942731 Class I Traditional
Decision Date
1994-10-13
Sponsor / Applicant
Shimadzu Corp.

Technical Specification

510(k) Submission ID K942731
Product Code IZO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1700
Decision Date 1994-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHIMAZU WHOLE BODY X-RAY CT SCANNER SCT-4800TF/GR received FDA 510(k) clearance under submission number K942731, sponsored by Shimadzu Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1994-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code IZO and 21 CFR 892.1700, within the Radiology review panel as a Class I device.