meddevicedb.com FDA Device Reference

MODEL 404-SP AND 504-SP INFUSION PUMPS MODIFIED

K912458 Class II Traditional
Decision Date
1991-06-24
Sponsor / Applicant
Medtronic Minimed

Technical Specification

510(k) Submission ID K912458
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1991-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 404-SP AND 504-SP INFUSION PUMPS MODIFIED received FDA 510(k) clearance under submission number K912458, 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 1991-06-24.

Classification & Regulation

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