PROBLOC, HN SERIES AND PROLONG, PL SERIES

PROBLOC, HN SERIES AND PROLONG, PL SERIES is an FDA 510(k)-cleared medical device (K050499) manufactured by Life-Tech, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 16, 2005. Regulation: 8.