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DUAL-ENERGY VERTEBRAL ASSESSMENT VIEW SOFTWARE

K023554 Class II Traditional
Decision Date
2002-12-20
Sponsor / Applicant
Ge Lunar Corp.

Technical Specification

510(k) Submission ID K023554
Product Code KGI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1170
Decision Date 2002-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUAL-ENERGY VERTEBRAL ASSESSMENT VIEW SOFTWARE received FDA 510(k) clearance under submission number K023554, sponsored by Ge Lunar 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 2002-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code KGI and 21 CFR 892.1170, within the Radiology review panel as a Class II device.