ALTERNATE PROCEDURE, PHARMACIA IGE EIA

ALTERNATE PROCEDURE, PHARMACIA IGE EIA is an FDA 510(k)-cleared medical device (K882616) 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 August 3, 1988. Regulation: 8.