KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345

KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345 is an FDA 510(k)-cleared medical device (K051258) 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 May 31, 2005. Regulation: 8.