GUIDE, WIRE, ANGIOGRAPHIC

GUIDE, WIRE, ANGIOGRAPHIC is an FDA 510(k)-cleared medical device (K850827) manufactured by Lake Region Mfg., 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 June 25, 1985. Regulation: 8.