AMPLANTZ AND BENTSON GUIDEWIRES

AMPLANTZ AND BENTSON GUIDEWIRES is an FDA 510(k)-cleared medical device (K912798) manufactured by Meadox Medicals, Div. Boston Scientific Corp.. 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 22, 1991. Regulation: 8.