
Scantibodies Laboratory, Inc.
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SYSCOS IDC - G, IDC, BSC, IDC - G is an FDA 510(k)-cleared medical device (K974262) manufactured by Scantibodies Laboratory, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 23, 1997. Regulation: 8.