meddevicedb.com FDA Device Reference

MINIMED(R) MODEL 506 EXTERNAL INSULIN PUMP

K901588 Class II Traditional
Decision Date
1990-07-02
Sponsor / Applicant
Medtronic Minimed

Technical Specification

510(k) Submission ID K901588
Product Code LZG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1990-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MINIMED(R) MODEL 506 EXTERNAL INSULIN PUMP received FDA 510(k) clearance under submission number K901588, sponsored by Medtronic Minimed. 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 1990-07-02.

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.