meddevicedb.com FDA Device Reference

DYE MANAGEMENT SYSTEM

K063784 Class II Special
Decision Date
2007-04-16
Sponsor / Applicant
Icu Medical, Inc.

Technical Specification

510(k) Submission ID K063784
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2007-04-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DYE MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K063784, sponsored by Icu Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-04-16.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.