SCHNEIDER MAGNUM PERIPHERAL RECANAL GUIDEWIRE

SCHNEIDER MAGNUM PERIPHERAL RECANAL GUIDEWIRE is an FDA 510(k)-cleared medical device (K912156) manufactured by Schneider Intl., Ltd.. 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 5, 1991. Regulation: 8.