QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE

QUICKWIRE - HYDROPHILIC COATED GUIDEWIRE is an FDA 510(k)-cleared medical device (K904582) manufactured by Meadox Surgimed, 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 February 24, 1991. Regulation: 8.