meddevicedb.com FDA Device Reference

MAGELLAN RATIO DISPENSER KIT

K041830 Class II Traditional
Decision Date
2004-09-29
Sponsor / Applicant
Medtronic Perfusion Systems

Technical Specification

510(k) Submission ID K041830
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2004-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAGELLAN RATIO DISPENSER KIT received FDA 510(k) clearance under submission number K041830, sponsored by Medtronic Perfusion Systems. 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 2004-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.