UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMH

UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMH is an FDA 510(k)-cleared medical device (K964152) manufactured by Pharmacia, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 22, 1997. Regulation: 8.