BIOTROL TOXO ELISA TEST M

BIOTROL TOXO ELISA TEST M is an FDA 510(k)-cleared medical device (K873293) manufactured by Biotrol, USA, 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 April 11, 1988. Regulation: 8.