FDA 510(k)

MFCD 2320

K-Number: K040158 · 2004-04-12

Decision Date2004-04-12

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MFCD 2320 is the device name listed in this FDA 510(k) record. The listed applicant is Barco N.V.. It received FDA 510(k) clearance on 2004-04-12 under 510(k) number K040158. 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 MFCD 2320?

MFCD 2320 is a medical device that received FDA 510(k) clearance on 2004-04-12. The listed applicant is Barco N.V.. The 510(k) number is K040158.

When did MFCD 2320 receive FDA 510(k) clearance?

MFCD 2320 received FDA 510(k) clearance on 2004-04-12, under 510(k) number K040158.

Who is the listed applicant for MFCD 2320?

The FDA 510(k) record lists Barco N.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MFCD 2320?

The FDA product code for MFCD 2320 is LLZ.

Other records listing Barco N.V. 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.