meddevicedb.com FDA Device Reference

HOSPIRA GEMSTAR INFUSION PUMP SYSTEM WITH HOSPIRA GEMSTAR SPRING ASSIST MECHANISM LOCKBOX-7 THERAPY

K051079 Class II Special
Decision Date
2005-05-19
Sponsor / Applicant
Hospicare, Inc.

Technical Specification

510(k) Submission ID K051079
Product Code MRZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2005-05-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOSPIRA GEMSTAR INFUSION PUMP SYSTEM WITH HOSPIRA GEMSTAR SPRING ASSIST MECHANISM LOCKBOX-7 THERAPY received FDA 510(k) clearance under submission number K051079, sponsored by Hospicare, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2005-05-19.

Classification & Regulation

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