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Halifax Biomedical, Inc.
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HALIFAX BIOMEDICAL TANATLUM BEAD SET is an FDA 510(k)-cleared medical device (K103417) manufactured by Halifax Biomedical, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 27, 2011. Regulation: 8.