FDA 510(k)

MAGELLAN RATIO DISPENSER KIT

K-Number: K041830 · 2004-09-29

Decision Date2004-09-29

Product CodeFMF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MAGELLAN RATIO DISPENSER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Perfusion Systems. It received FDA 510(k) clearance on 2004-09-29 under 510(k) number K041830. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGELLAN RATIO DISPENSER KIT?

MAGELLAN RATIO DISPENSER KIT is a medical device that received FDA 510(k) clearance on 2004-09-29. The listed applicant is Medtronic Perfusion Systems. The 510(k) number is K041830.

When did MAGELLAN RATIO DISPENSER KIT receive FDA 510(k) clearance?

MAGELLAN RATIO DISPENSER KIT received FDA 510(k) clearance on 2004-09-29, under 510(k) number K041830.

Who is the listed applicant for MAGELLAN RATIO DISPENSER KIT?

The FDA 510(k) record lists Medtronic Perfusion Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGELLAN RATIO DISPENSER KIT?

The FDA product code for MAGELLAN RATIO DISPENSER KIT is FMF.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.