
Barco N.V.
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BARCO MGD 221 2 MEGAPIXEL DIAGNOSTIC DISPLAY is an FDA 510(k)-cleared medical device (K000293) manufactured by Barco N.V.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 28, 2000. Regulation: 8.