
Eastman Kodak Company
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KODAK PRO-MEDICAL DIGITAL CAMERA SYSTEM is an FDA 510(k)-cleared medical device (K973430) manufactured by Eastman Kodak Company. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 16, 1998. Regulation: 8.