LOW POROSITY (LP) VASCULAR PROSTHESIS

LOW POROSITY (LP) VASCULAR PROSTHESIS is an FDA 510(k)-cleared medical device (K912911) manufactured by Intervascular, 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 September 22, 1991. Regulation: 8.