ENHANCE HUMAN SERUM ALBUMIN

ENHANCE HUMAN SERUM ALBUMIN is an FDA 510(k)-cleared medical device (K030850) manufactured by Conception Technologies. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 7, 2003. Regulation: 8.