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SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-4800TF

K935487 Class II Traditional
Decision Date
1994-07-05
Sponsor / Applicant
Shimadzu Corp.

Technical Specification

510(k) Submission ID K935487
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1994-07-05
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-4800TF received FDA 510(k) clearance under submission number K935487, 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 1994-07-05.

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.