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FDA 510(k)

BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE

K-Number: K982690 · 1998-10-06

ApplicantBarco N.V.
Decision Date1998-10-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE 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 1998-10-06 under 510(k) number K982690. 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 BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE?

BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE is a medical device that received FDA 510(k) clearance on 1998-10-06. The listed applicant is Barco N.V.. The 510(k) number is K982690.

When did BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE receive FDA 510(k) clearance?

BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE received FDA 510(k) clearance on 1998-10-06, under 510(k) number K982690.

Who is the listed applicant for BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE?

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 BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE?

The FDA product code for BARCO MEDICAL DISPLAY CONFORMITY AND CONSISTENCY SOFTWARE 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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