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FDA 510(k)

BARCOMED 2MP2

K-Number: K000015 · 2000-02-04

ApplicantBarco N.V.
Decision Date2000-02-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BARCOMED 2MP2 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 2000-02-04 under 510(k) number K000015. 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 BARCOMED 2MP2?

BARCOMED 2MP2 is a medical device that received FDA 510(k) clearance on 2000-02-04. The listed applicant is Barco N.V.. The 510(k) number is K000015.

When did BARCOMED 2MP2 receive FDA 510(k) clearance?

BARCOMED 2MP2 received FDA 510(k) clearance on 2000-02-04, under 510(k) number K000015.

Who is the listed applicant for BARCOMED 2MP2?

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 BARCOMED 2MP2?

The FDA product code for BARCOMED 2MP2 is LLZ.

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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.

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