ClearanceBrief
510(k) K140804 ยท DXX System, Catheter Control, Steerable

VDRIVE WITH V-LOOP/ VDRIVE DUO

ApplicantStereotaxis, Inc., Fairfax VA, US
DecisionSubstantially Equivalent, Sep 3, 2014
ReceivedMar 31, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140804

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.