DUAL LUMEN CATHETER, MODEL DL-35-90

DUAL LUMEN CATHETER, MODEL DL-35-90 is an FDA 510(k)-cleared medical device (K991601) manufactured by Endologix, 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 October 27, 1999. Regulation: 8.