meddevicedb.com FDA Device Reference

ADVANTAGE WINDOWS DIAGNOSTIC X-RAY WORKSTATION

K942120 Class II Traditional
Decision Date
1994-07-18
Sponsor / Applicant
GE Medical Systems

Technical Specification

510(k) Submission ID K942120
Product Code IZI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1600
Decision Date 1994-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANTAGE WINDOWS DIAGNOSTIC X-RAY WORKSTATION received FDA 510(k) clearance under submission number K942120, sponsored by GE 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 1994-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code IZI and 21 CFR 892.1600, within the Radiology review panel as a Class II device.