meddevicedb.com FDA Device Reference

ADVANTAGE WINDOWS VOLUME RENDERING OPTION

K972399 Class II Traditional
Decision Date
1997-09-23
Sponsor / Applicant
Ge Medical Systems, Inc.

Technical Specification

510(k) Submission ID K972399
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1997-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANTAGE WINDOWS VOLUME RENDERING OPTION received FDA 510(k) clearance under submission number K972399, sponsored by Ge Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-09-23.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.