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FDA 510(k)

CORONIS 3MP

K-Number: K131246 · 2013-05-24

ApplicantBarco N.V.
Decision Date2013-05-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORONIS 3MP 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 2013-05-24 under 510(k) number K131246. 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 CORONIS 3MP?

CORONIS 3MP is a medical device that received FDA 510(k) clearance on 2013-05-24. The listed applicant is Barco N.V.. The 510(k) number is K131246.

When did CORONIS 3MP receive FDA 510(k) clearance?

CORONIS 3MP received FDA 510(k) clearance on 2013-05-24, under 510(k) number K131246.

Who is the listed applicant for CORONIS 3MP?

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 CORONIS 3MP?

The FDA product code for CORONIS 3MP is LLZ.

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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.

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