meddevicedb.com FDA Device Reference

AMIGO INSULIN PUMP

K050312 Class II Traditional
Decision Date
2005-05-09
Sponsor / Applicant
Nipro Diabetes Systems, Inc.

Technical Specification

510(k) Submission ID K050312
Product Code LZG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2005-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMIGO INSULIN PUMP received FDA 510(k) clearance under submission number K050312, 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 2005-05-09.

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.