THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900

THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900 is an FDA 510(k)-cleared medical device (K913055) manufactured by Atomic Products Corp.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 5, 1991. Regulation: 8.