LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM

LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM is an FDA 510(k)-cleared medical device (K122397) manufactured by DiaSorin, 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 September 5, 2012. Regulation: 8.