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SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150K

K881795 Class I Traditional
Decision Date
1988-07-01
Sponsor / Applicant
Shimadzu Precision Instruments, Inc.

Technical Specification

510(k) Submission ID K881795
Product Code IZO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1700
Decision Date 1988-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150K received FDA 510(k) clearance under submission number K881795, sponsored by Shimadzu Precision Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1988-07-01.

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.