meddevicedb.com FDA Device Reference

IMAGEQUBE PACS

K051037 Class II Traditional
Decision Date
2005-06-28
Sponsor / Applicant
Intuitive Imaging Informatics, LLC

Technical Specification

510(k) Submission ID K051037
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2005-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGEQUBE PACS received FDA 510(k) clearance under submission number K051037, sponsored by Intuitive Imaging Informatics, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-06-28.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.