MAGNUM-MEIER RECANALIZATION GUIDEWIRE

MAGNUM-MEIER RECANALIZATION GUIDEWIRE is an FDA 510(k)-cleared medical device (K911547) 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 July 4, 1991. Regulation: 8.