MICROLITE TUBE LUMINOMETER #011-902-0000

MICROLITE TUBE LUMINOMETER #011-902-0000 is an FDA 510(k)-cleared medical device (K890502) manufactured by Dynatech Laboratories, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 26, 1989. Regulation: 8.