510(k) K180693

CoaguChek XS Pro System by Roche Diagnostics — Product Code GJS

K180693 is an FDA 510(k) premarket notification submitted by Roche Diagnostics for the device "CoaguChek XS Pro System". The FDA issued a decision of Substantially Equivalent on April 19, 2018. The device falls under product code GJS (Test, Time, Prothrombin), a Class II device regulated under 21 CFR 864.7750. Roche Diagnostics has at least 10 other 510(k) clearances on record.