SILVERSTREAK HYDROPHILIC GUIDEWIRE

SILVERSTREAK HYDROPHILIC GUIDEWIRE is an FDA 510(k)-cleared medical device (K982543) 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 December 10, 1998. Regulation: 8.