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Pan Probe Biotech, Inc.
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LIVESURE BARBITURATES SCREEN TEST is an FDA 510(k)-cleared medical device (K012133) manufactured by Pan Probe Biotech, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 19, 2001. Regulation: 8.