Y-ADAPTER W/THOUY BORST

Y-ADAPTER W/THOUY BORST is an FDA 510(k)-cleared medical device (K895580) manufactured by Angeion Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 29, 1990. Regulation: 8.