KODAK EKTASCAN DIGITAL INTERFACE/FOR AT&T

KODAK EKTASCAN DIGITAL INTERFACE/FOR AT&T is an FDA 510(k)-cleared medical device (K911405) manufactured by Eastman Kodak Company. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 22, 1991. Regulation: 8.