SCHNEIDER HYDRO-SIL GUIDEWIRE

SCHNEIDER HYDRO-SIL GUIDEWIRE is an FDA 510(k)-cleared medical device (K925804) manufactured by Schneider Intl., 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 February 11, 1993. Regulation: 8.