KODAK KODAFLEX II CASSETTE

KODAK KODAFLEX II CASSETTE is an FDA 510(k)-cleared medical device (K875083) 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 January 18, 1988. Regulation: 8.