IVT 0.014 GUIDE WIRE

IVT 0.014 GUIDE WIRE is an FDA 510(k)-cleared medical device (K895903) manufactured by Intensive Technology, 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 3, 1990. Regulation: 8.