QUIK-DOT TOXOPLASMOSIS

QUIK-DOT TOXOPLASMOSIS is an FDA 510(k)-cleared medical device (K890048) manufactured by Ampcor, 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 June 8, 1989. Regulation: 8.