FDA 510(k)

MRA-CMS

K-Number: K040746 · 2004-06-08

ApplicantMedis Medical Imaging Systems BV

Decision Date2004-06-08

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MRA-CMS is the device name listed in this FDA 510(k) record. The listed applicant is Medis Medical Imaging Systems BV. It received FDA 510(k) clearance on 2004-06-08 under 510(k) number K040746. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MRA-CMS?

MRA-CMS is a medical device that received FDA 510(k) clearance on 2004-06-08. The listed applicant is Medis Medical Imaging Systems BV. The 510(k) number is K040746.

When did MRA-CMS receive FDA 510(k) clearance?

MRA-CMS received FDA 510(k) clearance on 2004-06-08, under 510(k) number K040746.

Who is the listed applicant for MRA-CMS?

The FDA 510(k) record lists Medis Medical Imaging Systems BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MRA-CMS?

The FDA product code for MRA-CMS is LLZ.

Other records listing Medis Medical Imaging Systems BV as applicant

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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.