KODATROL I AND II CONTROL AND DILUENT SET

KODATROL I AND II CONTROL AND DILUENT SET is an FDA 510(k)-cleared medical device (K904768) manufactured by Eastman Kodak Company. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 8, 1990. Regulation: 8.