meddevicedb.com FDA Device Reference

IPACS CARDIO

K042781 Class II Traditional
Decision Date
2004-10-19
Sponsor / Applicant
Realtimeimage, Inc.

Technical Specification

510(k) Submission ID K042781
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2004-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IPACS CARDIO received FDA 510(k) clearance under submission number K042781, sponsored by Realtimeimage, 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 2004-10-19.

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.