KODAK MIN-R 2 CASSETTE

KODAK MIN-R 2 CASSETTE is an FDA 510(k)-cleared medical device (K890361) 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 February 23, 1989. Regulation: 8.