IMMULON 1 EIA TUBES, IMMULON 2 EIA TUBES

IMMULON 1 EIA TUBES, IMMULON 2 EIA TUBES is an FDA 510(k)-cleared medical device (K854423) manufactured by Dynatech Laboratories, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 19, 1985. Regulation: 8.