SPECIFIC ALLERGEN MODULES FOR ALASTAT ALLERGEN IGE

SPECIFIC ALLERGEN MODULES FOR ALASTAT ALLERGEN IGE is an FDA 510(k)-cleared medical device (K910075) manufactured by Diagnostic Products Corp.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 29, 1991. Regulation: 8.