
Dynatech Laboratories, Inc.
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MICROLITE ML 1000 (MODEL 3) MICROPLATE LUMINOMETER is an FDA 510(k)-cleared medical device (K895313) 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 October 16, 1989. Regulation: 8.