JUDO 1 Guidewire, JUDO 3 Guidewire, JUDO 6 Guidewire

JUDO 1 Guidewire, JUDO 3 Guidewire, JUDO 6 Guidewire is an FDA 510(k)-cleared medical device (K180795) manufactured by Boston Scientific. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 11, 2018. Regulation: 8.