meddevicedb.com FDA Device Reference

ADVANTAGE SIM

K951830 Class II Traditional
Decision Date
1995-11-13
Sponsor / Applicant
General Electric Co.

Technical Specification

510(k) Submission ID K951830
Product Code KPQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5840
Decision Date 1995-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANTAGE SIM received FDA 510(k) clearance under submission number K951830, sponsored by General Electric Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1995-11-13.

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.