MARDX LYME DISEASE EIA (IGG) TEST SYSTEM

MARDX LYME DISEASE EIA (IGG) TEST SYSTEM is an FDA 510(k)-cleared medical device (K894224) manufactured by Mardx Diagnostics, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 20, 1989. Regulation: 8.