PHARMACIA CAP SYSTEM IGE FEIA -- MODIFICATION

PHARMACIA CAP SYSTEM IGE FEIA -- MODIFICATION is an FDA 510(k)-cleared medical device (K923832) manufactured by Kabi 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 November 24, 1992. Regulation: 8.