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Eastman Kodak Company
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KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY is an FDA 510(k)-cleared medical device (K033821) manufactured by Eastman Kodak Company. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 19, 2004. Regulation: 8.