ASAHI PTCA GUIDE WIRE

ASAHI PTCA GUIDE WIRE is an FDA 510(k)-cleared medical device (K070945) 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 8, 2008. Regulation: 8.