BUCHBINDER(TM) MULTIFLEX(TM) GUIDEWIRE

BUCHBINDER(TM) MULTIFLEX(TM) GUIDEWIRE is an FDA 510(k)-cleared medical device (K862937) manufactured by Versaflex Delivery Systems, 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 September 23, 1986. Regulation: 8.