meddevicedb.com FDA Device Reference

QCT-BONE MINERAL ANALYSIS PHANTOM

K941126 Class II Traditional
Decision Date
1995-05-03
Sponsor / Applicant
Image Analysis, Inc.

Technical Specification

510(k) Submission ID K941126
Product Code KGI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1170
Decision Date 1995-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QCT-BONE MINERAL ANALYSIS PHANTOM received FDA 510(k) clearance under submission number K941126, sponsored by Image Analysis, 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 1995-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code KGI and 21 CFR 892.1170, within the Radiology review panel as a Class II device.