BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY
K-Number: K980541 · 1998-04-09
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Device Summary
Frequently Asked Questions
What is the BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY?
BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY is a medical device that received FDA 510(k) clearance on 1998-04-09. The listed applicant is Barco NV Display Systems. The 510(k) number is K980541.
When did BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY receive FDA 510(k) clearance?
BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY received FDA 510(k) clearance on 1998-04-09, under 510(k) number K980541.
Who is the listed applicant for BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY?
The FDA 510(k) record lists Barco NV Display Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY?
The FDA product code for BARCO MGD 521 5 MEGAPIXEL DIAGNOSTIC DISPLAY is LMD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Barco NV Display Systems as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LMD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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