meddevicedb.com FDA Device Reference

UNITY NETWORK IS PATIENT VIEWER

K032346 Class II Special
Decision Date
2003-08-05
Sponsor / Applicant
Ge Medical Systems Information Technologies

Technical Specification

510(k) Submission ID K032346
Product Code MSX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2003-08-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNITY NETWORK IS PATIENT VIEWER received FDA 510(k) clearance under submission number K032346, sponsored by Ge Medical Systems Information Technologies. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-08-05.

Classification & Regulation

This clearance is catalogued under FDA product code MSX and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.