FDA 510(k)

MFCD 118I

K-Number: K020059 · 2002-04-03

Decision Date2002-04-03

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MFCD 118I 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 2002-04-03 under 510(k) number K020059. 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 118I?

MFCD 118I is a medical device that received FDA 510(k) clearance on 2002-04-03. The listed applicant is Barco N.V.. The 510(k) number is K020059.

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

MFCD 118I received FDA 510(k) clearance on 2002-04-03, under 510(k) number K020059.

Who is the listed applicant for MFCD 118I?

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 118I?

The FDA product code for MFCD 118I 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.