
Sun Biomedical Laboratories, Inc.
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VISUALINE II (ALSO KNOWN AS SUNLINE) BARITURATES is an FDA 510(k)-cleared medical device (K014089) manufactured by Sun Biomedical Laboratories, 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 April 24, 2002. Regulation: 8.