meddevicedb.com FDA Device Reference

MaxZero Administration Sets

K143234 Class II Traditional
Decision Date
2014-11-20
Sponsor / Applicant
Care Fusion

Technical Specification

510(k) Submission ID K143234
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2014-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MaxZero Administration Sets received FDA 510(k) clearance under submission number K143234, sponsored by Care Fusion. 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 2014-11-20.

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.