SERUM, BLOOD UREA NITIOGEN

SERUM, BLOOD UREA NITIOGEN is an FDA 510(k)-cleared medical device (K781885) manufactured by Fisher Scientific Co., LLC. 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 December 19, 1978. Regulation: 8.