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SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150G

K952822 Class I Traditional
Decision Date
1995-07-12
Sponsor / Applicant
Shimadzu Corp.

Technical Specification

510(k) Submission ID K952822
Product Code IZO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1700
Decision Date 1995-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150G received FDA 510(k) clearance under submission number K952822, 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 1995-07-12.

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.