PUL,MONARY ARTERY VENT CATHETER

PUL,MONARY ARTERY VENT CATHETER is an FDA 510(k)-cleared medical device (K845046) manufactured by Dlp, Inc.. 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 2, 1985. Regulation: 8.