meddevicedb.com FDA Device Reference

GLUCOPRO EVO INFUSION PUMP

K013309 Class II Traditional
Decision Date
2002-06-24
Sponsor / Applicant
Nipro Diabetes Systems, Inc.

Technical Specification

510(k) Submission ID K013309
Product Code LZG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2002-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLUCOPRO EVO INFUSION PUMP received FDA 510(k) clearance under submission number K013309, sponsored by Nipro Diabetes Systems, 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 2002-06-24.

Classification & Regulation

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