MEDRAD PATHFINDER-E ROADMAPPING SYSTEM

MEDRAD PATHFINDER-E ROADMAPPING SYSTEM is an FDA 510(k)-cleared medical device (K922274) manufactured by Medrad, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 8, 1992. Regulation: 8.