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FDA 510(k)

CORONIS 5MP

K-Number: K111990 · 2011-10-17

ApplicantBarco N.V.
Decision Date2011-10-17
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CORONIS 5MP 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 2011-10-17 under 510(k) number K111990. 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 5MP?

CORONIS 5MP is a medical device that received FDA 510(k) clearance on 2011-10-17. The listed applicant is Barco N.V.. The 510(k) number is K111990.

When did CORONIS 5MP receive FDA 510(k) clearance?

CORONIS 5MP received FDA 510(k) clearance on 2011-10-17, under 510(k) number K111990.

Who is the listed applicant for CORONIS 5MP?

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 5MP?

The FDA product code for CORONIS 5MP 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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