meddevicedb.com FDA Device Reference

ADVANTAGE SIM 6.0

K021780 Class II Traditional
Decision Date
2002-07-29
Sponsor / Applicant
General Electric Medical Systems

Technical Specification

510(k) Submission ID K021780
Product Code KPQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5840
Decision Date 2002-07-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANTAGE SIM 6.0 received FDA 510(k) clearance under submission number K021780, sponsored by General Electric 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 2002-07-29.

Classification & Regulation

This clearance is catalogued under FDA product code KPQ and 21 CFR 892.5840, within the Radiology review panel as a Class II device.