SHEEP BLOOD IN ALSEVER'S, CITR., DEFIBR

SHEEP BLOOD IN ALSEVER'S, CITR., DEFIBR is an FDA 510(k)-cleared medical device (K812376) manufactured by Dutchland Laboratories, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 8, 1981. Regulation: 8.