INTERSEPT 1375 VENOUS RESERVOIR

INTERSEPT 1375 VENOUS RESERVOIR is an FDA 510(k)-cleared medical device (K903632) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 1990. Regulation: 8.