510(k) K180795

JUDO 1 Guidewire, JUDO 3 Guidewire, JUDO 6 Guidewire by Boston Scientific — Product Code DQX

K180795 is an FDA 510(k) premarket notification submitted by Boston Scientific for the device "JUDO 1 Guidewire, JUDO 3 Guidewire, JUDO 6 Guidewire". The FDA issued a decision of Substantially Equivalent on Apr 12, 2018. The device falls under product code DQX (Wire, Guide, Catheter), a Class II device regulated under 21 CFR 870.1330. Boston Scientific has 493 other 510(k) clearances on record.