KODAK AMERLITE TOTAL THYROID CONTROL SERA

KODAK AMERLITE TOTAL THYROID CONTROL SERA is an FDA 510(k)-cleared medical device (K923740) 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 September 24, 1992. Regulation: 8.