HUMAN A-DS DNA EIA KIT FOR DIAGNOSTIC USE

HUMAN A-DS DNA EIA KIT FOR DIAGNOSTIC USE is an FDA 510(k)-cleared medical device (K930247) manufactured by The Binding Site, Ltd.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 9, 1993. Regulation: 8.