BIOTIS MODIFIED THAYER MARTIN

BIOTIS MODIFIED THAYER MARTIN is an FDA 510(k)-cleared medical device (K860384) manufactured by Otisville Biotech, 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 February 23, 1986. Regulation: 8.