
Diasorin S.P.A
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DIASORIN LIAISON CMV IGM/IGG is an FDA 510(k)-cleared medical device (K040290) manufactured by Diasorin S.P.A. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 31, 2005. Regulation: 8.