meddevicedb.com FDA Device Reference

EXPERT-XL TOTAL BODY ACQUISITION AND ANALYSIS SOFTWARE

K965226 Class II Traditional
Decision Date
1997-10-03
Sponsor / Applicant
Lunar Corp.

Technical Specification

510(k) Submission ID K965226
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1997-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXPERT-XL TOTAL BODY ACQUISITION AND ANALYSIS SOFTWARE received FDA 510(k) clearance under submission number K965226, sponsored by Lunar Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1997-10-03.

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.