
Zeus Scientific, Inc.
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ZEUS ELISA CARDIOLIPIN IGG/IGM/IGA TEST SYSTEM is an FDA 510(k)-cleared medical device (K102425) manufactured by Zeus Scientific, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 11, 2011. Regulation: 8.