TERUMO CORONARY GUIDE WIRE

TERUMO CORONARY GUIDE WIRE is an FDA 510(k)-cleared medical device (K925852) manufactured by Terumo Medical 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 June 9, 1993. Regulation: 8.