meddevicedb.com FDA Device Reference

ADVANCE ANALYSIS SOFTWARE

K941223 Class II Traditional
Decision Date
1994-11-29
Sponsor / Applicant
General Electric Co.

Technical Specification

510(k) Submission ID K941223
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1994-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANCE ANALYSIS SOFTWARE received FDA 510(k) clearance under submission number K941223, 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 1994-11-29.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.