KODAK AMERLITE CK-MB CONTROL SERA LAN.4413

KODAK AMERLITE CK-MB CONTROL SERA LAN.4413 is an FDA 510(k)-cleared medical device (K925880) 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 February 4, 1993. Regulation: 8.