meddevicedb.com FDA Device Reference

ADVANTAGE SIM MD

K052345 Class II Traditional
Decision Date
2005-09-14
Sponsor / Applicant
GE Healthcare

Technical Specification

510(k) Submission ID K052345
Product Code KPQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5840
Decision Date 2005-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANTAGE SIM MD received FDA 510(k) clearance under submission number K052345, sponsored by GE Healthcare. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-09-14.

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.