DHBTI-ALLERGEN IGE FASTSCREEN IV (G1,G5,G12,G13)

DHBTI-ALLERGEN IGE FASTSCREEN IV (G1,G5,G12,G13) is an FDA 510(k)-cleared medical device (K883273) manufactured by 3M Company. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 6, 1988. Regulation: 8.