ASAHI PTCA GUIDE WIRE, J SHAPE SERIES

ASAHI PTCA GUIDE WIRE, J SHAPE SERIES is an FDA 510(k)-cleared medical device (K043422) 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, 2005. Regulation: 8.