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SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-5000TX

K911501 Class II Traditional
Decision Date
1991-07-17
Sponsor / Applicant
Shimadzu Medical Systems

Technical Specification

510(k) Submission ID K911501
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1991-07-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-5000TX received FDA 510(k) clearance under submission number K911501, 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 1991-07-17.

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.