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Eastman Kodak Company
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KODAK DIRECTVIEW TABLETOP CASSETTE is an FDA 510(k)-cleared medical device (K013686) 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 December 6, 2001. Regulation: 8.