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Arbor Vita Corportation
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AVC A/H5N1 FLU TEST is an FDA 510(k)-cleared medical device (K083278) manufactured by Arbor Vita Corportation. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 7, 2009. Regulation: 8.