GI MOTILITY TEST MEDIUM W/TTC

GI MOTILITY TEST MEDIUM W/TTC is an FDA 510(k)-cleared medical device (K863603) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 29, 1986. Regulation: 8.