ASAHI ULTIMATEBROS 3 PTCA GUIDE WIRE

ASAHI ULTIMATEBROS 3 PTCA GUIDE WIRE is an FDA 510(k)-cleared medical device (K101986) 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 September 8, 2011. Regulation: 8.