0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE

0.016 GUIDE WIRE FOR NEUROLOGICAL ENDOSCOPE is an FDA 510(k)-cleared medical device (K913074) 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 November 4, 1991. Regulation: 8.