meddevicedb.com FDA Device Reference

MILLENNIUM HUBER PLUS SAFETY INFUSION SET

K993848 Class II Traditional
Decision Date
2000-01-27
Sponsor / Applicant
Millennium Medical Distribution, Inc.

Technical Specification

510(k) Submission ID K993848
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2000-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILLENNIUM HUBER PLUS SAFETY INFUSION SET received FDA 510(k) clearance under submission number K993848, sponsored by Millennium Medical Distribution, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2000-01-27.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.