meddevicedb.com FDA Device Reference

QCT-LUNG NODULE (TM) ANALYSIS PACKAGE

K891931 Class II Traditional
Decision Date
1989-05-18
Sponsor / Applicant
Image Analysis, Inc.

Technical Specification

510(k) Submission ID K891931
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1989-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QCT-LUNG NODULE (TM) ANALYSIS PACKAGE received FDA 510(k) clearance under submission number K891931, 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 1989-05-18.

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.