KODAK MN-R 2000 CASSETTE

KODAK MN-R 2000 CASSETTE is an FDA 510(k)-cleared medical device (K961453) 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 July 24, 1996. Regulation: 8.