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SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-120

K963617 Class II Traditional
Decision Date
1996-11-08
Sponsor / Applicant
Shimadzu Medical Systems

Technical Specification

510(k) Submission ID K963617
Product Code JAA
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 1996-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-120 received FDA 510(k) clearance under submission number K963617, 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 1996-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.