meddevicedb.com FDA Device Reference

SHIMADZU WHOLE BODY X-RAY COMPUTED TOMOGRAPHY SCANNER SCT-6800TH

K973327 Class II Traditional
Decision Date
1997-10-08
Sponsor / Applicant
Shimadzu Medical Systems

Technical Specification

510(k) Submission ID K973327
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1997-10-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHIMADZU WHOLE BODY X-RAY COMPUTED TOMOGRAPHY SCANNER SCT-6800TH received FDA 510(k) clearance under submission number K973327, sponsored by Shimadzu Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-10-08.

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.