INTERVENTIONAL PRODUCTS - GUIDE WIRES

INTERVENTIONAL PRODUCTS - GUIDE WIRES is an FDA 510(k)-cleared medical device (K890207) manufactured by E-Z-Em, 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 May 30, 1989. Regulation: 8.