DYNATECH MR 300 MANUAL MICROELISA

DYNATECH MR 300 MANUAL MICROELISA is an FDA 510(k)-cleared medical device (K874244) 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 November 2, 1987. Regulation: 8.