
Diamond Diagnostics, Inc.
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MISSION TRINITY R (LEVEL 1) (LEVEL 2) (LEVEL 3), (LEVEL 1,2,3) is an FDA 510(k)-cleared medical device (K093384) manufactured by Diamond Diagnostics, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 9, 2010. Regulation: 8.