PRINCETON BIOMEDIX URICASE (UV)

PRINCETON BIOMEDIX URICASE (UV) is an FDA 510(k)-cleared medical device (K780859) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 26, 1978. Regulation: 8.