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LifeCare PCA Infusion System

K143612 Class II Traditional
Decision Date
2016-04-08
Sponsor / Applicant
Hospira, Inc.

Technical Specification

510(k) Submission ID K143612
Product Code MEA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2016-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LifeCare PCA Infusion System received FDA 510(k) clearance under submission number K143612, sponsored by Hospira, 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 2016-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code MEA and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.