MULTI-ALLERGEN IGE FASTSCREEN V (T1,T3,T5,T7,T10)

MULTI-ALLERGEN IGE FASTSCREEN V (T1,T3,T5,T7,T10) is an FDA 510(k)-cleared medical device (K883371) 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 October 26, 1988. Regulation: 8.