
Cytotech, Inc.
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CYTOTECH C1-INHIBITOR ENZYME IMMUNOASSAY is an FDA 510(k)-cleared medical device (K872426) manufactured by Cytotech, 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 July 22, 1987. Regulation: 8.