IQ UREA NITROGEN

IQ UREA NITROGEN is an FDA 510(k)-cleared medical device (K863901) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 23, 1986. Regulation: 8.