ASAHI GUIDE WIRE EXTENSION, MODEL AG149000

ASAHI GUIDE WIRE EXTENSION, MODEL AG149000 is an FDA 510(k)-cleared medical device (K083145) manufactured by Asahi Intecc Co., Ltd.. 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 11, 2009. Regulation: 8.