SCIMED AVENUE CORONARY GUIDEWIRE INSERTION TOOL

SCIMED AVENUE CORONARY GUIDEWIRE INSERTION TOOL is an FDA 510(k)-cleared medical device (K922410) manufactured by Scimed Life Systems, 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 July 22, 1992. Regulation: 8.