MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608

MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608 is an FDA 510(k)-cleared medical device (K002212) manufactured by Micro Therapeutics, 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 August 2, 2000. Regulation: 8.