
Iquum, Inc.
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LIAT (TM) INFLUENZA A / B ASSAY, LIAT (TM) ANALYZER is an FDA 510(k)-cleared medical device (K111387) manufactured by Iquum, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 3, 2011. Regulation: 8.