FDA 510(k)

MFCD 118

K-Number: K000291 · 2000-03-27

Decision Date2000-03-27

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MFCD 118 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 2000-03-27 under 510(k) number K000291. 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 118?

MFCD 118 is a medical device that received FDA 510(k) clearance on 2000-03-27. The listed applicant is Barco N.V.. The 510(k) number is K000291.

When did MFCD 118 receive FDA 510(k) clearance?

MFCD 118 received FDA 510(k) clearance on 2000-03-27, under 510(k) number K000291.

Who is the listed applicant for MFCD 118?

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 118?

The FDA product code for MFCD 118 is LLZ.

Other records listing Barco N.V. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.