TELEFLEX STEERABLE GUIDEWIRE

TELEFLEX STEERABLE GUIDEWIRE is an FDA 510(k)-cleared medical device (K871850) manufactured by Teleflexmedical, 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 January 26, 1988. Regulation: 8.