
Instrumentation Laboratory CO
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IL TEST LAC SCREEN (CLAIMS ADDED TO ACL FUTURA), IL TEST LAC CONFIRM (CLAIMS ADDAD TO ACL FUTURA) is an FDA 510(k)-cleared medical device (K990302) manufactured by Instrumentation Laboratory CO. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 7, 1999. Regulation: 8.