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Medical Analysis Systems, Inc.
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TRI-POINT LIQUIMMUNE LIQUID ASSAYED CONTROL LEVELS 1,2, AND 3 is an FDA 510(k)-cleared medical device (K011731) manufactured by Medical Analysis Systems, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 4, 2001. Regulation: 8.