HIGH TORQUE TEMPORARY PERVENOUS LEAD W/DEPTH MARK

HIGH TORQUE TEMPORARY PERVENOUS LEAD W/DEPTH MARK is an FDA 510(k)-cleared medical device (K882045) manufactured by Cordis Leads, 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 July 11, 1988. Regulation: 8.