LP200 & HP800 SERIES VASCULAR PROSTH

LP200 & HP800 SERIES VASCULAR PROSTH is an FDA 510(k)-cleared medical device (K833716) 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 January 9, 1984. Regulation: 8.