meddevicedb.com FDA Device Reference

MODIFICATION TO UNITY NETWORK ID

K033672 Class II Special
Decision Date
2003-12-18
Sponsor / Applicant
Ge Medical Systems Information Technologies

Technical Specification

510(k) Submission ID K033672
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2003-12-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO UNITY NETWORK ID received FDA 510(k) clearance under submission number K033672, 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 2003-12-18.

Classification & Regulation

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