
Lorenz Biotech S.P.A.
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LORENZ BIOTECH APTIVA, VERSION 2.13 is an FDA 510(k)-cleared medical device (K061828) manufactured by Lorenz Biotech S.P.A.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 23, 2007. Regulation: 8.