meddevicedb.com FDA Device Reference

OPTIV ANTAGE DH POWER INJECTION SYSTEM

K042744 Class II Special
Decision Date
2004-11-30
Sponsor / Applicant
Mallinckrodt Inc., Liebel-Flarsheim Business

Technical Specification

510(k) Submission ID K042744
Product Code DXT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 2004-11-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTIV ANTAGE DH POWER INJECTION SYSTEM received FDA 510(k) clearance under submission number K042744, sponsored by Mallinckrodt Inc., Liebel-Flarsheim Business. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code DXT and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.