SCHNEIDER MAGNARAIL PROBING CATHETER

SCHNEIDER MAGNARAIL PROBING CATHETER is an FDA 510(k)-cleared medical device (K910259) 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 April 17, 1991. Regulation: 8.